Detergent compositions having a specific hydrophobic peroxyacid bleaching system and anionic surfactant

ABSTRACT

Granular detergent compositions, particularly phosphate-containing detergent compositions, contain a specific hydrophobic peroxyacid bleaching system and a specific anionic surfactant system. The compositions are suitable for use in laundry washing methods.

TECHNICAL FIELD

The present invention relates to granular detergent compositions and in particular phosphate-containing detergent compositions, which comprise a specific hydrophobic peroxyacid bleaching system and a specific anionic surfactant system. The compositions are suitable for use in laundry washing methods.

BACKGROUND TO THE INVENTION

In the past decades research efforts have been directed towards the development of bleaching systems, based on organic peroxyacids, which can provide effective stain and/or soil removal from fabrics at lower wash temperatures. The organic peroxyacids are often obtained by the in situ perhydrolysis of organic peroxyacid bleach precursor compounds (bleach activators).

A commonly employed precursor compound is tetraacetyl ethylene diamine (TAED) which provides effective hydrophilic cleaning especially on beverage stains. Further organic peroxyacid precursors have thus been developed to deal with hydrophobic stains and soils.

However, to achieve effective bleaching of a detergent, both hydrophobic and hydrophilic stains need to be bleached by the bleach system. Furthermore, to achieve an effective or efficient bleach system, the system should provide excellent bleaching at low levels, thereby minimizing the chance of damage to the fabrics.

Thus, there is a need to provide detergent compositions which comprise low levels of a bleaching system, containing a bleach system, which has a very effective bleaching performance, having an excellent performance at both hydrophobic soils and hydrophilic soils.

Most conventional detergent compositions contain mixtures of various detersive surfactant components. Commonly encountered surfactant components include various anionic surfactants, especially the alkyl benzene sulphonates, alkyl sulfates, alkyl alkoxy sulfates and various nonionic surfactants, such as alkyl ethoxylates and alkylphenol ethoxylates.

The inventors have now surprisingly found that the introduction in detergent compositions comprising a hydrophobic bleaching system and one or more mono-functionalised anionic sulphate or/and sulphonate surfactant components, of specific anionic surfactants, which are relatively more-functionalised, results in an improved cleaning performance. Namely, in particular, anionic surfactants which are more-functionalised because they have more than one anionic charge or they have hydrophilic (substituent) groups or they have another anionic charge which is not a head group, have been found to improve the bleaching and cleaning performance of the detergent compositions containing a specific hydrophobic bleaching system and the additional mono-functionalised anionic surfactant. Without wishing to be bound by theory, it is believed that the use of relatively hydrophilic anionic surfactant facilitates the selective migration of one or more of the components of the hydrophobic bleaching system to the bleachable stains or soils specifically. It is believed that these more-functionalised anionic surfactant form effectively CO-micelles with the hydrophobic bleaching system, more easily than mono-functionalised surfactants. It is believed that this can facilitate the dissolution/dispersion of the hydrophobic bleaching system. Thereby, these components can efficiently bleach both hydrophilic and hydrophobic soils.

Thus, a low level of the hydrophobic bleaching system and the specific surfactant system can be used to achieve efficient and excellent bleaching and cleaning performance. Furthermore, surprisingly it has been found that the cleaning performance of these detergent compositions is achieved for a wide variety of stains and soils.

All documents cited in the present description are, in relevant part, incorporated herein by reference.

SUMMARY OF THE INVENTION

The present invention relates to a detergent composition comprising:

(a) from 1% to 70%, preferably from 10% to 30% by weight of an anionic surfactant system, comprising:

(i) at least 50% by weight of the system of one or more alkyl mono-sulphate and/or mono-sulphonate surfactant; and

(ii) one or more additional anionic surfactants selected from the group comprising:

(I) an alkyl ester sulphonate surfactant of formula

R¹—CH(SO₃M)—(A)_(x)—C(O)—OR²

 wherein R¹ is a C₆-C₂₂ hydrocarbyl, R² is a C₁-C₆ alkyl, A is a C₆-C₂₂ alkylene, alkenylene, x is 0 or 1, and M is a cation;

(II) a dianionic surfactant of formula

 where R is an, optionally substituted, alkyl, alkyl, alkenyl, aryl, alkaryl, ether, ester, amine or amide group of chain length C₁ to C₂₈, or hydrogen; A and B are independently selected from alkylene, alkenylene, (poly)alkoxylene, hydroxyalkylene, arylalkylene or amido alkylene groups of chain length C₁ to C₂₈; whereby A, B, and R in total contain from 4 to about 31 carbon atoms; X and Y are anionic groups from the group comprising, carboxylate, sulfate and sulfonate, preferably least one of X or Y is a sulfate group; z is 0 or 1; and M is a cationic counterion;

(III) an alkyl alkoxylated sulphate of formula

R⁵O(A)_(m)SO₄M

 wherein R⁵ is a C₆-C₂₄ alkyl or hydroxyalkyl group, A is an alkoxy unit, preferably ethoxy or propoxy, the average of m is at least 5, preferably at least 9 and M is a cationic counterion; and

b) from 0.01% to 10.0%, preferably from 0.5% to 4% by weight of the composition of a hydrophobic bleaching system comprising

(i) a percarboxylic acid of formula

R¹—CO₃M

 wherein R¹ has at least 6 carbon atoms, and M is a counterion; or

(ii) a percarboxylic acid precursor of formula

R¹—CO—L

 wherein L is a leaving group which is linked to the R¹—CO— group with an oxygen atom, and R¹ has at least 6 carbon atoms; or mixtures of (i) and (ii) with the proviso that when the more-functionalised anionic surfactant is a dianionic surfactant of formula (11), wherein R has 18 or 20 C-atoms which, is present at a level of 2% or 2.7% by weight of the composition, the weight ratio of said dianionic surfactant to the hydrophobic bleaching agent is not 1:1 or 1.35:1.

Preferably the detergent composition is a solid, preferably granular, phosphate-containing detergent composition.

DETAILED DESCRIPTION OF THE INVENTION

The detergent compositions of the invention comprise an anionic surfactant system containing one or more alkyl mono-sulphate or mono-sulphonate surfactants and one or more additional anionic surfactants of formula (I), (II) and (III) above.

The anionic surfactant system is present in the composition at a level of from 1% to 70% by weight of the composition, preferably from 10% to 30%, more preferably from 12% to 25% by weight of the composition.

The more-functionalised sulphate and sulphonate surfactants are present at least at a level of 50%, but more preferably at a level of at least 60%, most preferably of from 70% to 85% by weight of the system.

The weight ratio of the anionic surfactant system to the hydrophobic bleaching system is preferably from 1:10 to 100:1, more preferably from 1:1 to 80:1, more preferably from 1:1 to 50:1, most preferably from 5:1 to 30:1.

Anionic Alkyl Mono-sulphate Surfactant

The anionic mono-sulphate surfactants in accordance with the invention include the linear and branched primary and secondary alkyl sulphates, alkyl ethoxysulphates having an average ethoxylation number of 3 or below, fatty oleoyl glycerol sulphates, alkyl phenol ethylene oxide ether sulphates, the C₅-C₁₇ acyl-N—(C₁-C₄ alkyl) and —N—(C₁-C₂ hydroxyalkyl)glucamine sulphates, and sulphates of alkylpolysaccharides.

Primary alkyl mono-sulphate surfactants are preferably selected from the linear and branched primary C_(10-C) ₁₈ alkyl sulphates, more preferably the C₁-C₁₅ branched chain alkyl sulphates and the C₁₂-C₁₄ linear chain alkyl sulphates.

Preferred secondary alkyl mono-sulphate surfactant are of the formula

R³—CH(SO₄M)—R⁴

wherein R³ is a C₈-C₂₀ hydrocycarbyl, R⁴ is a hydrocycarbyl and M is a cation.

Alkyl ethoxy mono-sulphate surfactants are preferably selected from the group consisting of the C₁₀-C₁₈ alkyl sulphates which have been ethoxylated with from 0.5 to 3 moles of ethylene oxide per molecule. More preferably, the alkyl ethoxysulphate surfactant is a C₁₁-C₁₈, most preferably C₁₁-C₁₅ alkyl sulphate which has been ethoxylated with from 0.5 to 3, preferably from 1 to 3, moles of ethylene oxide per molecule.

A particularly preferred aspect of the invention employs mixtures of the preferred alkyl sulphate and alkyl ethoxysulphate surfactants. Preferred salts are sodium and potassium salts.

The mono-sulphate surfactants are preferably present at a level of from 1% to 20%, more preferably from 2% to 15%, most preferably from 2.5% to 10% by weight of the composition.

Anionic Mono-sulphonate Surfactant

The anionic mono-sulphonate surfactants in accordance with the invention include the salts of C₅-C₂₀ linear alkylbenzene sulphonates, alkyl ester sulphonates, C₆-C₂₂ primary or secondary alkane sulphonates, C₆-C₂₄ olefin sulphonates, sulphonated polycarboxylic acids, and any mixtures thereof. Highly preferred is a C12-C16 linear alkylbenzene sulphonate. Preferred salts are sodium and potassium salts.

The mono-sulphonate surfactants are preferably present at a level of from 1% to 30%, more preferably from 5% to 25%, most preferably from 5% to 20% by weight of the composition.

Alkyl Ester Sulphonate Surfactant

The alkyl ester sulphonated surfactant of the invention is of the formula

R¹—CH(SO₃M)—(A)_(x)—C(O)—OR²

wherein R¹ is a C₆-C₂₂ hydrocarbyl, R² is a C₁-C₆ alkyl, A is a C₆-C₂₂ alkylene, alkenylene, x is 0 or 1, and M is a cation. The counterion M is preferably sodium, potassium or ammonium.

The alkyl ester sulphonated surfactant is preferably a α-sulpho alkyl ester of the formula above, whereby thus x is 0. Preferably, R¹ is an alkyl or alkenyl group of from 10 to 22, preferably 16 C atoms and x is preferably 0. R² is preferably ethyl or more preferably methyl.

It can be preferred that the R¹ of the ester is derived from unsaturated fatty acids, with preferably 1, 2 or 3 double bonds. It can also be preferred that R¹ of the ester is derived from a natural occurring fatty acid, preferably palmic acid or stearic acid or mixtures thereof.

The alkyl ester sulphonated surfactant is preferably present at a level of from 0.1% to 25%, more preferably from 0.5% to 15%, more preferably from 0.7 to 5%, most preferably from 1.0% to 2.0% by weight of the composition. Preferred alkyl ester sulphonated surfactants and processes for making them are described in for example EP 355675 A1.

Dianionic Surfactants

The dianionic surfactants, of the present invention are of the formula:

where R is an, optionally substituted, alkyl, alkenyl, aryl, alkaryl, ether, ester, amine or amide group of chain length C₁ to C₂₈, preferably C₃ to C₂₄, most preferably C₈ to C₂₀, or hydrogen; A and B are independently selected from alkylene, alkenylene, (poly)alkoxylene, hydroxyalkylene, arylalkylene or amido alkylene groups of chain length C₁ to C₂₈ preferably C₁ to C₅, most preferably C₁ or C₂, or a covalent bond, and preferably A and B in total contain at least 2 atoms; A, B, and R in total contain from 4 to about 31 carbon atoms; X and Y are anionic groups selected from the group comprising carboxylate, and preferably sulfate and sulfonate, z is 0 or preferably 1; and M is a cationic moiety, preferably a substituted or unsubstituted ammonium ion, or an alkali or alkaline earth metal ion.

The most preferred dianionic surfactant has the formula as above where R is an alkyl group of chain length from C₁₀ to C₁₈, A and B are independently C₁ or C₂, both X and Y are sulfate groups, and M is a potassium, ammonium, or a sodium ion.

The dianionic surfactant is typically present at levels of incorporation of from about 0.1% to about 20%, preferably from about 0.3% to about 10%, most preferably from about 0.5% to about 5% by weight of the detergent composition.

Preferred dianionic surfactants herein include:

(a) 3 disulphate compounds, preferably 1,3 C7-C23 (i.e., the total number of carbons in the molecule) straight or branched chain alkyl or alkenyl disulphates, more preferably having the formula:

 wherein R is a straight or branched chain alkyl or alkenyl group of chain length from about C₄ to about C₂₀;

(b) 1,4 disulphate compounds, preferably 1,4 C8-C22 straight or branched chain alkyl or alkenyl disulphates, more preferably having the formula:

 wherein R is a straight or branched chain alkyl or alkenyl group of chain length from about C₄ to about C₁₈; preferred R are selected from octanyl, nonanyl, decyl, dodecyl, tetradecyl, hexadecyl, octadecyl, and mixtures thereof; and

(c) 1,5 disulphate compounds, preferably 1,5 C9-C23 straight or branched chain alkyl or alkenyl disulphates, more preferably having the formula:

 wherein R is a straight or branched chain alkyl or alkenyl group of chain length from about C₄ to about C₁₈.

It can be preferred that the dianionic surfactants of the invention are alkoxylated dianionic surfactants.

The alkoxylated dianionic surfactants of the invention comprise a structural skeleton of at least five carbon atoms, to which two anionic substituent groups spaced at least three atoms apart are attached. At least one of said anionic substituent groups is an alkoxy-linked sulphate or sulphonate group. Said structural skeleton can for example comprise any of the groups consisting of alkyl, substituted alkyl, alkenyl, aryl, alkaryl, ether, ester, amine and amide groups. Preferred alkoxy moieties are ethoxy, propoxy, and combinations thereof.

The structural skeleton preferably comprises from 5 to 32, preferably 7 to 28, most preferably 12 to 24 atoms. Preferably the structural skeleton comprises only carbon-containing groups and more preferably comprises only hydrocarbyl groups. Most preferably the structural skeleton comprises only straight or branched chain alkyl groups.

The structural skeleton is preferably branched. Preferably at least 10% by weight of the structural skeleton is branched and the branches are preferably from 1 to 5, more preferably from 1 to 3, most preferably from 1 to 2 atoms in length (not including the sulphate or sulphonate group attached to the branching).

A preferred alkoxylated dianionic surfactant has the formula

where R is an, optionally substituted, alkyl, alkenyl, aryl, alkaryl, ether, ester, amine or amide group of chain length C₁ to C₂₈, preferably C₃ to C₂₄, most preferably C₈ to C₂₀, or hydrogen; A and B are independently selected from, optionally substituted, alkyl and alkenyl group of chain length C₁ to C₂₈, preferably C₁ to C₅, most preferably C₁ or C₂, or a covalent bond; EO/PO are alkoxy moieties selected from ethoxy, propoxy, and mixed ethoxy/propoxy groups, wherein n and m are independently within the range of from about 0 to about 10, with at least m or n being at least 1; A and B in total contain at least 2 atoms; A, B, and R in total contain from 4 to about 31 carbon atoms; X and Y are anionic groups selected from the group consisting of sulphate and sulphonate, provided that at least one of X or Y is a sulfate group; and M is a cationic moiety, preferably a substituted or unsubstituted ammonium ion, or an alkali or alkaline earth metal ion.

The most preferred alkoxylated dianionic surfactant has the formula as above where R is an alkyl group of chain length from C₁₀ to C₁₈, A and B are independently C₁ or C₂, n and m are both 1, both X and Y are sulfate groups, and M is a potassium, ammonium, or a sodium ion.

The alkoxylated dianionic cleaning agent is typically present at levels of incorporation of from about 0.1% to about 20%, preferably from about 0.3% to about 15%, most preferably from about 0.5% to about 10% by weight of the bleaching detergent composition.

Preferred alkoxylated dianionic surfactants herein include:

ethoxylated and/or propoxylated disulphate compounds, preferably C10-C24 straight or branched chain alkyl or alkenyl ethoxylated and/or propoxylated disulphates, more preferably having the formulae:

 wherein R is a straight or branched chain alkyl or alkenyl group of chain length from about C6 to about C₁₈; EO/PO are alkoxy moieties selected from ethoxy, propoxy, and mixed ethoxy/propoxy groups; and n and m are independently within the range of from about 0 to about 10 (preferably from about 0 to about 5), with at least m or n being 1.

Alkoxylated Alkyl Surfactant

The alkoxylated alkl sulphate of the invention is of formula

R⁵O(A)_(m)SO₄M

wherein R⁵ is an, optionally substituted C₆-C₂₄ alkyl or hydroxyalkyl or alkenyl group having a C₁₀-C₂₄ alkyl component, A is an alkoxy unit, preferably ethoxy or propoxy, the average of m is at least 5, preferably at least 9; and M is a cationic counterion.

Preferably, m is 11 or above, more preferably from 11 to 20.

M is preferably sodium, potassium or ammonium.

Hydrophobic Bleaching System

An essential feature of detergent compositions of the invention is a hydrophobic bleaching system, present at a level of from 0.1% to 10% by, more preferably from 0.01% to 4% by weight, even more preferably from 0.1% to 4% by weight, most preferably from 0.5% to 3% by weight of the composition.

The bleaching system comprising a percarboxylic acid precursor and/or a percarboxylic acid, of the formulas (b)(i) and (b)(ii) as defined above, which are hydrophobic compounds.

Preferably such organic compounds are those whose parent carboxylic acid has a critical micelle concentration less than 0.5 moles/liter and wherein said critical micelle concentration is measured in aqueous solution at 20°-50° C.

The percarboxylic acid formed from the precursor or the peroxy acid contains at least 7 carbon atoms, more preferably from 7 to 12 carbon atoms, more preferably from 8 to 11 carbon atoms, most preferably 9 or 10 carbon atoms. Thus, wherein R¹ in the defined formula of (b)(I) and (b)(ii) contains at least 6, preferably from 6 to 11, more preferably from 7 to 10, most preferably 8 or 9 carbon atoms. In a preferred aspect the percarboxylic acid formed from the precursor or the peroxy acid has an alkyl chain comprising at least 7 carbon atoms, more preferably at least 8 carbon atoms, most preferably 9 carbon atoms.

Percarboxylic acid bleach precursor are compounds which react with hydrogen peroxide in a perhydrolysis reaction to produce a percarboxylic acid.

The counterion M of the percarboxylic acid is preferably sodium, potassium or hydrogen.

Preferably the detergent compositions of the invention comprise in combination with the hydrophobic bleaching system of the invention a source of hydrogen peroxide as described below. The provision of the percarboxylic acid occurs then by an in situ reaction of a (the) precursor with a source of hydrogen peroxide.

Compositions containing mixtures of a hydrogen peroxide source and a percarboxylic acid precursor in combination with a preformed peroxy acid are also envisaged.

Percarboxylic Acid Precursor

The percarboxylic acid precursor can be any ester which had been described as a bleach activator for use in laundry detergents, for instance alkyl percarboxylic acid precursors described herein, sugar esters, such as pentaacetylglucose, esters of imidic acids such as ethyl benzimidate triacylcyanurates, such as triacetylcyanurate and tribenzoylcyanurate an esters giving relatively surface active oxidising products for instance of C₈₋₁₈-alkanoic or -aralkanoic acids such as described in GB-A-864798, GB-A-1147871 and the esters described in EP-A-98129 and EP-A-106634.

Alkyl Percarboxylic Acid Bleach Precursors

Alkyl percarboxylic acid bleach precursors are highly preferred precursors for the present invention.

Preferred can be phenyl esters of C₁₄₋₂₂-alkanoic or alkenoic acids, esters of hydroxylamine, geminal diesters of lower alkanoic acids and gem-idols, such as those described in EP-A-0125781 especially 1,1,5-triacetoxypent-4-ene and 1,1,5,5-tetraacetoxypentane and the corresponding butene and butane compounds, ethylidene benzoate acetate and bis(ethylidene acetate)adipate and enol esters, for instance as described in EP-A-0140648 and EP-A-0092932.

Other highly preferred alkyl percarboxylic acid precursors include decanoyloxy-benzenesulphonate sodium salt (DOBS), benzoyloxy-benzenesulphonate sodium salt (BOBS), more preferred sodium 3,5,5-tri-methyl hexanoyloxybenzene sulfonate (iso-NOBS) and even more preferred sodium nonanoyloxybenzene sulfonate (NOBS).

The percarboxylic acid precursor compounds present in the bleaching system are preferably incorporated at a level of from 0.05% to 20% by weight, more preferably from 0.1% to 15% by weight, most preferably from 0.2% to 10% by weight of the detergent compositions.

Leaving Groups

The percarboxylic acid precursor of the invention comprises a leaving group L. The leaving group L group must be sufficiently reactive for the perhydrolysis reaction to occur within the optimum time frame (e.g., a wash cycle). However, if L is too reactive, this activator will be difficult to stabilize for use in a bleaching composition.

Preferred L groups are selected from the group consisting of:

and mixtures thereof, R³ is an alkyl chain containing from 1 to 8 carbon atoms, R⁴ is H or R³, and Y is H or a solubilizing group. Any of R³ and R⁴ may be substituted by essentially any functional group including, for example alkyl, hydroxy, alkoxy, halogen, amine, nitrosyl, amide and ammonium or alkyl ammonium groups.

The preferred solubilizing groups are —SO₃ ⁻M⁺, —CO₂ ⁻M⁺, —SO₄ ⁻M⁺, —N⁺(R³)₄X⁻ and O←N(R³)₃ and most preferably —SO₃ ⁻M⁺ and —CO₂ ⁻M⁺ wherein R³ is an alkyl chain containing from 1 to 4 carbon atoms, M is a cation which provides solubility to the bleach activator and X is an anion which provides solubility to the bleach activator. Preferably, M is an alkali metal, ammonium or substituted ammonium cation, with sodium and potassium being most preferred, and X is a halide, hydroxide, methylsulfate or acetate anion.

Preformed Organic Peroxy Acid

The bleaching system may contain as an alternative to the precursors mentioned above, or in addition to, a preformed peroxy acid, typically at a level of from 0.05% to 20% by weight, more preferably from 1% to 10% by weight of the detergent composition.

When the preformed peroxy acid is an alternative to the precursors mentioned above, and preferably when the preformed peroxy acid is present in addition to the precursors mentioned above, the peroxy acid has the general formula:

R¹—CO₃M

wherein R¹ has at least 6 carbon atoms, and M is a counterion.

A preferred class of peroxy acid compounds are the amide substituted compounds of the following general formulae:

wherein R¹ is an aryl or alkaryl group with from about 1 to about 14 carbon atoms, R² is an alkylene, arylene, and alkarylene group containing from about 1 to 14 carbon atoms, and R⁵ is H or an alkyl, aryl, or alkaryl group containing 1 to 10 carbon atoms. R¹ preferably contains from about 6 to 12 carbon atoms. R² preferably contains from about 4 to 8 carbon atoms. R¹ may be straight chain or branched alkyl, substituted aryl or alkylaryl containing branching, substitution, or both and may be sourced from either synthetic sources or natural sources including for example, tallow fat. Analogous structural variations are permissible for R². R² can include alkyl, aryl, wherein said R² may also contain halogen, nitrogen, sulphur and other typical substituent groups or organic compounds. R⁵ is preferably H or methyl. R¹ and R⁵ should not contain more than 18 carbon atoms total. Amide substituted bleach activator compounds of this type are described in EP-A-0170386. Suitable examples of this class of agents include (6-octylamino)-6-oxo-caproic acid, (6-nonylamino)-6-oxo-caproic acid, (6-decylamino)-6-oxo-caproic acid, magnesium monoperoxyphthalate hexahydrate, the salt of metachloro perbenzoic acid, 4-nonylamino-4-oxoperoxybutyric acid and diperoxydodecanedioic acid. Such bleaching agents are disclosed in U.S. Pat. No. 4,483,781, U.S. Pat. No. 4,634,551, EP 0,133,354, U.S. Pat. No. 4,412,934 and EP 0,170,386.

A preferred preformed peroxyacid bleach compound for the purpose of the invention is monononylamido peroxycarboxylic acid.

Other suitable organic peroxyacids include diperoxyalkanedioc acids having more than 7 carbon atoms, such as diperoxydodecanedioc acid (DPDA), diperoxytetradecanedioc acid and diperoxyhexadecanedioc acid. Mono- and diperazelaic acid, mono- and diperbrassylic acid and N-phthaloylaminoperoxicaproic acid (PAP), nonanoylamido peroxo-adipic acid (NAPAA) and hexane sulphenoyl peroxypropionic acid and are also suitable herein.

Other suitable organic peroxyacids include diamino peroxyacids, which are disclosed in WO 95/03275, with the following general formula:

wherein:

R is selected from the group consisting of C₁-C₁₂ alkylene, C₅-C₁₂ cycloalkylene, C₆-C₁₂ arylene and radical combinations thereof;

R¹ and R² are independently selected from the group consisting of H, C₁-C₁₆ alkyl and C₆-C₁₂ aryl radicals and a radical that can form a C₃-C₁₂ ring together with R³ and both nitrogens; R³ is selected from the group consisting of C₁-C₁₂ alkylene, C₅-C₁₂ cycloalkylene and C₆-C₁₂ arylene radicals; n and n′ each are an integer chosen such that the sum thereof is 1; m and m′ each are an integer chosen such that the sum thereof is 1; and

M is selected from the group consisting of H, alkali metal, alkaline earth metal, ammonium, alkanolammonium cations and radicals and combinations thereof

Other suitable organic peroxyacids are include the amido peroxyacids which are disclosed in WO 95/16673, with the following general structure:

X—Ar—CO—NY—R(Z)—CO—OOH

in which X represents hydrogen or a compatible substituent, Ar is an aryl group, R represents (CH₂)_(n) in which n=2 or 3, and Y and Z each represent independently a substituent selected from hydrogen or an alkyl or aryl or alkaryl group or an aryl group substituted by a compatible substituent provided that at least one of Y and Z is not hydrogen if n=3. The substituent X on the benzene nucleus is preferably a hydrogen or a meta or para substituent, selected from the group comprising halogen, typically chlorine atom, or some other non-released non-interfering species such as an alkyl group, conveniently up to C6 for example a methyl, ethyl or propyl group. Alternatively, X can represent a second amido-percarboxylic acid substituent of formula:

CO—NY—R(Z)—CO—OOH

in which R, Y, Z and n are as defined above.

Inorganic Perhydrate Bleaches

Inorganic perhydrate salts are a preferred source of hydrogen peroxide. These salts are normally incorporated in the form of the alkali metal, preferably sodium salt at a level of from 1% to 40% by weight, more preferably from 2% to 30% by weight and most preferably from 5% to 25% by weight of the compositions.

Examples of inorganic perhydrate salts include perborate, percarbonate, perphosphate, persulfate and persilicate salts. The inorganic perhydrate salts are normally the alkali metal salts. The inorganic perhydrate salt may be included as the crystalline solid without additional protection. For certain perhydrate salts however, the preferred executions of such granular compositions utilize a coated form of the material which provides better storage stability for the perhydrate salt in the granular product. Suitable coatings comprise inorganic salts such as alkali metal silicate, carbonate or borate salts or mixtures thereof, or organic materials such as waxes, oils, or fatty soaps.

Sodium perborate is a preferred perhydrate salt and can be in the form of the monohydrate of nominal formula NaBO₂H₂O₂ or the tetrahydrate NaBO₂H₂O₂.3H₂O.

Alkali metal percarbonates, particularly sodium percarbonate are preferred perhydrates herein. Sodium percarbonate is an addition compound having a formula corresponding to 2Na₂CO₃.3H₂O₂, and is available commercially as a crystalline solid.

Potassium peroxymonopersulfate is another inorganic perhydrate salt of use in the detergent compositions herein.

Additional Detergent Components

The detergent compositions or components thereof in accord with the invention may also contain additional detergent components. The precise nature of these additional components, and levels of incorporation thereof will depend on the physical form of the composition or component, and the precise nature of the washing operation for which it is to be used.

The compositions or components thereof, of the invention preferably contain one or more additional detergent components selected from additional surfactants, additional bleaches, bleach catalysts, alkalinity systems, builders, phosphate-containing builders, organic polymeric compounds, enzymes, suds suppressors, lime soap, dispersants, soil suspension and anti-redeposition agents soil releasing agents, perfumes, brightners, photobleaching agents and additional corrosion inhibitors.

Additional Bleach System Components

Preferred alkyl percarboxylic precursor compounds of the imide type include the N—,N,N¹N¹ tetra acetylated alkylene diamines wherein the alkylene group contains at least 7 carbon atoms.

Preferred additional components of the bleaching system comprised in the detergent compositions of the invention peroxyacid precursors are amide substituted alkyl peroxyacid precursor compounds, including those of the following general formulae:

wherein R¹ is an aryl or alkaryl group with from about 1 to about 14 carbon atoms, R² is an alkylene, arylene, and alkarylene group containing from about 1 to 14 carbon atoms, and R⁵ is H or an alkyl, aryl, or alkaryl group containing 1 to 10 carbon atoms and L can be essentially any leaving group. R¹ preferably contains from about 6 to 12 carbon atoms. R² preferably contains from about 4 to 8 carbon atoms. R¹ may be straight chain or branched alkyl, substituted aryl or alkylaryl containing branching, substitution, or both and may be sourced from either synthetic sources or natural sources including for example, tallow fat. Analogous structural variations are permissible for R². R² can include alkyl, aryl, wherein said R² may also contain halogen, nitrogen, sulphur and other typical substituent groups or organic compounds. R⁵ is preferably H or methyl. R¹ and R⁵ should not contain more than 18 carbon atoms total. Amide substituted bleach activator compounds of this type are described in EP-A-0170386.

Preferred examples of bleach precursors of this type include amide substituted peroxyacid precursor compounds selected from (6-octanamido-caproyl)oxybenzenesulfonate, (6-decanamido-caproyl)oxybenzene-sulfonate, and the highly preferred (6-nonanamidocaproyl)oxybenzenesulfonate, and mixtures thereof as described in EP-A-0170386.

Also suitable additional precursor compounds are of the benzoxazin-type, as disclosed for example in EP-A-332,294 and EP-A-482,807, particularly those having the formula:

wherein R₁ is an alkyl, alkaryl, aryl, or arylalkyl containing at least 5 carbon atoms.

Bleach Catalyst

The bleach system can contain a transition metal containing bleach catalyst.

One suitable type of bleach catalyst is a catalyst system comprising a transition metal cation of defined bleach catalytic activity, such as copper, iron or manganese cations, an auxiliary metal cation having little or no bleach catalytic activity, such as zinc or aluminum cations, and a sequestrant having defined stability constants for the catalytic and auxiliary metal cations, particularly ethylenediaminetetraacetic acid, ethylenediaminetetra(methylenephosphonic acid) and water-soluble salts thereof. Such catalysts are disclosed in U.S. Pat. No. 4,430,243.

Other types of bleach catalysts include the manganese-based complexes disclosed in U.S. Pat. No. 5,246,621 and U.S. Pat. No. 5,244,594. Preferred examples of these catalysts include Mn^(IV) ₂(u-O)₃(1,4,7-trimethyl-1,4,7-triazacyclononane)₂-(PF₆)₂, Mn^(III) ₂(u-O)₁(u-OAc)₂(1,4,7-trimethyl-1,4,7-triazacyclononane)₂-(ClO₄)₂, Mn^(IV) ₄(u-O)₆(1,4,7-triazacyclononane)₄-(ClO₄)₂, Mn^(III)Mn^(IV) ₄(u-O)₁(u-OAc)₂-(1,4,7-trimethyl-1,4,7-triazacyclononane)₂-(ClO₄)₃, and mixtures thereof. Others are described in European patent application publication no. 549,272. Other ligands suitable for use herein include 1,5,9-trimethyl-1,5,9-triazacyclododecane, 2-methyl-1,4,7-triazacyclononane, 2-methyl-1,4,7-triazacyclononane, 1,2,4,7-tetramethyl-1,4,7-triazacyclononane, and mixtures thereof.

The bleach catalysts useful herein may also be selected as appropriate for the present invention. For examples of suitable bleach catalysts see U.S. Pat. No. 4,246,612 and U.S. Pat. No. 5,227,084. See also U.S. Pat. No. 5,194,416 which teaches mononuclear manganese (IV) complexes such as Mn(1,4,7-trimethyl-1,4,7-triazacyclononane)(OCH₃)₃-(PF₆).

Still another type of bleach catalyst, as disclosed in U.S. Pat. No. 5,114,606, is a water-soluble complex of manganese (III), and/or (IV) with a ligand which is a non-carboxylate polyhydroxy compound having at least three consecutive C—OH groups. Preferred ligands include sorbitol, iditol, dulsitol, mannitol, xylithol, arabitol, adonitol, meso-erythritol, meso-inositol, lactose, and mixtures thereof

U.S. Pat. No. 5,114,611 teaches a bleach catalyst comprising a complex of transition metals, including Mn, Co, Fe, or Cu, with an non-(macro)-cyclic ligand. Said ligands are of the formula:

wherein R¹, R², R³, and R⁴ can each be selected from H, substituted alkyl and aryl groups such that each R¹—N═C—R² and R³—C═N—R⁴ form a five or six-membered ring. Said ring can further be substituted. B is a bridging group selected from O, S. CR⁵R⁶, NR⁷ and C═O, wherein R⁵, R⁶, and R⁷ can each be H, alkyl, or aryl groups, including substituted or unsubstituted groups. Preferred ligands include pyridine, pyridazine, pyrimidine, pyrazine, imidazole, pyrazole, and triazole rings. Optionally, said rings may be substituted with substituents such as alkyl, aryl, alkoxy, halide, and nitro. Particularly preferred is the ligand 2,2′-bispyridylamine. Preferred bleach catalysts include Co, Cu, Mn, Fe, -bispyridylmethane and -bispyridylamine complexes. Highly preferred catalysts include Co(2,2′-bispyridylamine)Cl₂, Di(isothiocyanato)bispyridylamine-cobalt(II), trisdipyridylamine-cobalt(II)perchlorate, Co(2,2-bispyridylamine)₂O₂ClO₄, Bis-(2,2′-bispyridylamine)copper(II)perchlorate, tris(di-2-pyridylamine) iron(II)perchlorate, and mixtures thereof.

Other examples include binuclear Mn complexed with tetra-N-dentate and bi-N-dentate ligands, including N₄Mn^(III)(u-O)₂Mn^(IV)N₄)⁺ and [Bipy₂Mn^(III)(u-O)₂Mn^(IV)bipy₂]-(ClO₄)₃.

Other bleach catalysts are described, for example, in European patent application, publication no. 408,131 (cobalt complex catalysts), European patent applications, publication nos. 384,503, and 306,089 (metallo-porphyrin catalysts), U.S. Pat. No. 4,728,455 (manganese/multidentate ligand catalyst), U.S. Pat. No. 4,711,748 and European patent application, publication no. 224,952, (absorbed manganese on aluminosilicate catalyst), U.S. Pat. No. 4,601,845 (aluminosilicate support with manganese and zinc or magnesium salt), U.S. Pat. No. 4,626,373 (manganese/ligand catalyst), U.S. Pat. No. 4,119,557 (ferric complex catalyst), German Pat. specification 2,054,019 (cobalt chelant catalyst) Canadian 866,191 (transition metal-containing salts), U.S. Pat. No. 4,430,243 (chelants with manganese cations and non-catalytic metal cations), and U.S. Pat. No. 4,728,455 (manganese gluconate catalysts).

The bleach catalyst is typically used in a catalytically effective amount in the compositions and processes herein. By “catalytically effective amount” is meant an amount which is sufficient, under whatever comparative test conditions are employed, to enhance bleaching and removal of the stain or stains of interest from the target substrate. The test conditions will vary, depending on the type of washing appliance used and the habits of the user. Some users elect to use very hot water; others use warm or even cold water in laundering operations. Of course, the catalytic performance of the bleach catalyst will be affected by such considerations, and the levels of bleach catalyst used in fully-formulated detergent and bleach compositions can be appropriately adjusted. As a practical matter, and not by way of limitation, the compositions and processes herein can be adjusted to provide on the order of at least one part per ten million of the active bleach catalyst species in the aqueous washing liquor, and will preferably provide from about 1 ppm to about 200 ppm of the catalyst species in the wash liquor. To illustrate this point further, on the order of 3 micromolar manganese catalyst is effective at 40° C., pH 10 under European conditions using perborate and a bleach precursor. An increase in concentration of 3-5 fold may be required under U.S. conditions to achieve the same results.

Surfactant

The detergent compositions or components thereof in accord with the invention preferably contain one or more additional surfactants selected from nonionic, cationic, ampholytic, amphoteric and zwitterionic surfactants and mixtures thereof

A typical listing of nonionic, ampholytic, and zwitterionic classes, and species of these surfactants, is given in U.S. Pat. No. 3,929,678 issued to Laughlin and Heuring on Dec. 30, 1975. Further examples are given in “Surface Active Agents and Detergents” (Vol. I and II by Schwartz, Perry and Bereb). A list of suitable cationic surfactants is given in U.S. Pat. No. 4,259,217 issued to Murphy on Mar. 31, 1981.

Alkoxylated Nonionic Surfactant

Essentially any alkoxylated nonionic ic surfactants are suitable herein. The ethoxylated and propoxylated nonionic surfactants are preferred.

Preferred alkoxylated surfactants can be selected from the classes of the nonionic condensates of alkyl phenols, nonionic ethoxylated alcohols, nonionic ethoxylated/propoxylated fatty alcohols, nonionic ethoxylate/propoxylate condensates with propylene glycol, and the nonionic ethoxylate condensation products with propylene oxide/ethylene diamine adducts.

Nonionic Alkoxylated Alcohol Surfactant

The condensation products of aliphatic alcohols with from 1 to 25 moles of alkylene oxide, particularly ethylene oxide and/or propylene oxide, are suitable for use herein. The alkyl chain of the aliphatic alcohol can either be straight or branched, primary or secondary, and generally contains from 6 to 22 carbon atoms. Particularly preferred are the condensation products of alcohols having an alkyl group containing from 8 to 20 carbon atoms with from 2 to 10 moles of ethylene oxide per mole of alcohol.

Nonionic Polyhydroxy Fatty Acid Amide Surfactant

Polyhydroxy fatty acid amides suitable for use herein are those having the structural formula R²CONR¹Z wherein: R1 is H, C₁-C₄ hydrocarbyl, 2-hydroxy ethyl, 2-hydroxy propyl, ethoxy, propoxy, or a mixture thereof, preferable C₁-C₄ alkyl, more preferably C₁ or C₂ alkyl, most preferably C₁ alkyl (i.e., methyl); and R₂ is a C₅-C₃₁ hydrocarbyl, preferably straight-chain C₅-C₁₉ alkyl or alkenyl, more preferably straight-chain C₉-C₁₇ alkyl or alkenyl, most preferably straight-chain C₁₁-C₁₇ alkyl or alkenyl, or mixture thereof; and Z is a polyhydroxyhydrocarbyl having a linear hydrocarbyl chain with at least 3 hydroxyls directly connected to the chain, or an alkoxylated derivative (preferably ethoxylated or propoxylated) thereof. Z preferably will be derived from a reducing sugar in a reductive amination reaction; more preferably Z is a glycityl.

Nonionic Fatty Acid Amide Surfactant

Suitable fatty acid amide surfactants include those having the formula: R⁶CON(R⁷)₂ wherein R⁶ is an alkyl group containing from 7 to 21, preferably from 9 to 17 carbon atoms and each R⁷ is selected from the group consisting of hydrogen, C₁-C₄ alkyl, C₁-C₄ hydroxyalkyl, and —(C₂H₄O)_(x)H, where x is in the range of from 1 to 3.

Nonionic Alkylpolysaccharide Surfactant

Suitable alkylpolysaccharides for use herein are disclosed in U.S. Pat. No. 4,565,647, Llenado, issued Jan. 21, 1986, having a hydrophobic group containing from 6 to 30 carbon atoms and a polysaccharide, e.g., a polyglycoside, hydrophilic group containing from 1.3 to 10 saccharide units.

Preferred alkylpolyglycosides have the formula:

R²O(C_(n)H_(2n)O)t(glycosyl)_(x)

wherein R² is selected from the group consisting of alkyl, alkylphenyl, hydroxyalkyl, hydroxyalkylphenyl, and mixtures thereof in which the alkyl groups contain from 10 to 18 carbon atoms; n is 2 or 3; t is from 0 to 10, and x is from 1.3 to 8. The glycosyl is preferably derived from glucose.

Amphoteric Surfactant

Suitable amphoteric surfactants for use herein include the amine oxide surfactants and the alkyl amphocarboxylic acids.

Suitable amine oxides include those compounds having the formula R³(OR⁴)_(x)N₀(R⁵)₂ wherein R³ is selected from an alkyl, hydroxyalkyl, acylamidopropoyl and alkyl phenyl group, or mixtures thereof, containing from 8 to 26 carbon atoms; R⁴ is an alkylene or hydroxyalkylene group containing from 2 to 3 carbon atoms, or mixtures thereof; x is from 0 to 5, preferably from 0 to 3; and each R⁵ is an alkyl or hydroxyalkyl group containing from 1 to 3, or a polyethylene oxide group containing from 1 to 3 ethylene oxide groups. Preferred are C₁₀-C₁₈ alkyl dimethylamine oxide, and C₁₀₋₁₈ acylamido alkyl dimethylamine oxide.

A suitable example of an alkyl aphodicarboxylic acid is Miranol(™) C2M Conc. manufactured by Miranol, Inc., Dayton, N.J.

Zwitterionic Surfactant

Zwitterionic surfactants can also be incorporated into the detergent compositions or components thereof in accord with the invention. These surfactants can be broadly described as derivatives of secondary and tertiary amines, derivatives of heterocyclic secondary and tertiary amines, or derivatives of quaternary ammonium, quaternary phosphonium or tertiary sulfonium compounds. Betaine and sultaine surfactants are exemplary zwitterionic surfactants for use herein.

Suitable betaines are those compounds having the formula R(R′)₂N⁺R²COO⁻ wherein R is a C₆-C₁₈ hydrocarbyl group, each R¹ is typically C₁-C₃ alkyl, and R² is a C₁-C₅ hydrocarbyl group. Preferred betaines are C₁₂₋₁₈ dimethyl-ammonio hexanoate and the C₁₀₋₁₈ acylamidopropane (or ethane) dimethyl (or diethyl) betaines. Complex betaine surfactants are also suitable for use herein.

Cationic Surfactants

Suitable cationic surfactants to be used in the detergent compositions or components thereof herein include the quaternary ammonium surfactants. Preferably the quaternary ammonium surfactant is a mono C₆-C₁₆, preferably C₆-C₁₀ N-alkyl or alkenyl ammonium surfactants wherein the remaining N positions are substituted by methyl, hydroxyethyl or hydroxypropyl groups. Preferred are also the mono-alkoxylated and bis-alkoxylated amine surfactants.

Another suitable group of cationic surfactants which can be used in the detergent compositions or components thereof herein are cationic ester surfactants. The cationic ester surfactant is a, preferably water dispersible, compound having surfactant properties comprising at least one ester (i.e. —COO—) linkage and at least one cationically charged group.

Suitable cationic ester surfactants, including choline ester surfactants, have for example been disclosed in U.S. Pat. Nos. 4,228,042, 4,239,660 and 4,260,529.

In one preferred aspect the ester linkage and cationically charged group are separated from each other in the surfactant molecule by a spacer group consisting of a chain comprising at least three atoms (i.e. of three atoms chain length), preferably from three to eight atoms, more preferably from three to five atoms, most preferably three atoms. The atoms forming the spacer group chain are selected from the group consisting of carbon, nitrogen and oxygen atoms and any mixtures thereof, with the proviso that any nitrogen or oxygen atom in said chain connects only with carbon atoms in the chain. Thus spacer groups having, for example, —O—O— (i.e. peroxide), —N—N—, and —N—O— linkages are excluded, whilst spacer groups having, for example —CH₂—O—CH₂— and —CH₂—NH—CH₂— linkages are included. In a preferred aspect the spacer group chain comprises only carbon atoms, most preferably the chain is a hydrocarbyl chain.

Cationic Mono-alkoxylated Amine Surfactants

The cationic mono-alkoxylated amine surfactant are preferably of the general formula I:

wherein R¹ is an alkyl or alkenyl moiety containing from about 6 to about 18 carbon atoms, preferably 6 to about 16 carbon atoms, most preferably from about 6 to about 14 carbon atoms; R² and R³ are each independently alkyl groups containing from one to about three carbon atoms, preferably methyl, most preferably both R² and R³ are methyl groups; R⁴ is selected from hydrogen (preferred), methyl and ethyl; X⁻ is an anion such as chloride, bromide, methylsulfate, sulfate, or the like, to provide electrical neutrality; A is a alkoxy group, especially a ethoxy, propoxy or butoxy group; and p is from 0 to about 30, preferably 2 to about 15, most preferably 2 to about 8, with the proviso that if A is ethoxy and R₄ is hydrogen and p is 1, R¹ is not a C₁₂-C₁₄ alkyl group.

Preferably the ApR⁴ group in formula I has p=1 and is a hydroxyalkyl group, having no greater than 6 carbon atoms whereby the —OH group is separated from the quaternary ammonium nitrogen atom by no more than 3 carbon atoms. Particularly preferred ApR⁴ groups are —CH₂CH₂OH, —CH₂CH₂CH₂OH, —CH₂CH(CH₃)OH and —CH(CH₃)CH₂OH, with —CH₂CH₂OH being particularly preferred. Preferred R¹ groups no greater than 10 carbon atoms, or even no greater than 8 or 9 carbon atoms. Preferred R¹ groups are linear alkyl groups. Linear R¹ groups having from 8 to 11 carbon atoms, or from 8 to 10 carbon atoms are preferred. Such a cationic surfactant which is highly preferred has a formula wherein R₁ is a C₈-C₁₀ alkyl group, p is 1, A is ethoxy and R₂ and R₃ are methyl groups.

Another highly preferred cationic mono-alkoxylated amine surfactants for use herein are of the formula

wherein R¹ is C₁₀-C₁₈ hydrocarbyl and mixtures thereof, especially C₁₀-C₁₄ alkyl, preferably C₁₀ and C₁₂ alkyl, and X is any convenient anion to provide charge balance, preferably chloride or bromide.

As noted, compounds of the foregoing type include those wherein the ethoxy (CH₂CH₂O) units (EO) are replaced by butoxy, isopropoxy [CH(CH₃)CH₂O] and [CH₂CH(CH₃O] units (i-Pr) or n-propoxy units (Pr), or mixtures of EO and/or Pr and/or i-Pr units.

The levels of the cationic mono-alkoxylated amine surfactants used in detergent compositions of the invention is preferably from 0.1% to 20%, more preferably from 0.4% to 7%, most preferably from 0.5% to 3.0% by weight of the composition.

Cationic bis-Alkoxylated Amine Surfactant

The cationic bis-alkoxylated amine surfactant preferably has the general formula II:

wherein R¹ is an alkyl or alkenyl moiety containing from about 8 to about 18 carbon atoms, preferably 10 to about 16 carbon atoms, most preferably from about 10 to about 14 carbon atoms; R² is an alkyl group containing from one to three carbon atoms, preferably methyl; R³ and R⁴ can vary independently and are selected from hydrogen (preferred), methyl and ethyl, X⁻ is an anion such as chloride, bromide, methylsulfate, sulfate, or the like, sufficient to provide electrical neutrality. A and A′ can vary independently and are each selected from C₁-C₄ alkoxy, especially ethoxy, (i.e., —CH₂CH₂O—), propoxy, butoxy and mixtures thereof; p is from 1 to about 30, preferably 1 to about 4 and q is from 1 to about 30, preferably 1 to about 4, and most preferably both p and q are 1.

Highly preferred cationic bis-alkoxylated amine surfactants for use herein are of the formula

wherein R¹ is C₁₀-C₁₈ hydrocarbyl and mixtures thereof, preferably C₁₀, C₁₂, C₁₄ alkyl and mixtures thereof. X is any convenient anion to provide charge balance, preferably chloride. With reference to the general cationic bis-alkoxylated amine structure noted above, since in a preferred compound R¹ is derived from (coconut) C₁₂-C₁₄ alkyl fraction fatty acids, R² is methyl and ApR³ and A′qR⁴ are each monoethoxy.

Other cationic bis-alkoxylated amine surfactants useful herein include compounds of the formula:

wherein R¹ is C₁₀-C₁₈ hydrocarbyl, preferably C₁₀-C₁₄ alkyl, independently p is 1 to about 3 and q is 1 to about 3, R² is C₁-C₃ alkyl, preferably methyl, and X is an anion, especially chloride or bromide.

Other compounds of the foregoing type include those wherein the ethoxy (CH₂CH₂O) units (EO) are replaced by butoxy (Bu) isopropoxy [CH(CH₃)CH₂O] and [CH₂CH(CH₃O] units (i-Pr) or n-propoxy units (Pr), or mixtures of EO and/or Pr and/or i-Pr units.

The levels of the cationic bis-alkoxylated amine surfactants used in detergent compositions of the invention is preferably from 0.1% to 20%, more preferably from 0.4% to 7%, most preferably from 0.5% to 3.0% by weight of the composition.

Optional Surfactants

Suitable optional soap surfactants include the secondary soap surfactants which contain a carboxyl unit connected to a secondary carbon. Preferred secondary soap surfactants for use herein are water-soluble members selected from the group consisting of the water-soluble salts of 2-methyl-1-undecanoic acid, 2-ethyl-1-decanoic acid, 2-propyl-1-nonanoic acid, 2-butyl-1-octanoic acid and 2-pentyl-1-heptanoic acid. Certain soaps may also be included as suds suppressors.

Other optional additional anionic surfactants are the carboxylate-based anionic surfactants known in the art and alkali metal sarcosinates of formula R—CON(R¹)CH₂COOM, wherein R is a C₅-C₁₇ linear or branched alkyl or alkenyl group, R¹ is a C₁-C₄ alkyl group and M is an alkali metal ion. Preferred examples are the myristyl and oleoyl methyl sarcosinates in the form of their sodium salts

Water-soluble Builder Compound

The detergent compositions or components thereof in accord with the present invention preferably contain a water-soluble builder compound, typically present in detergent compositions at a level of from 1% to 80% by weight, preferably from 10% to 70% by weight, most preferably from 20% to 60% by weight of the composition.

The detergent compositions of the invention preferably comprise phosphate-containing builder material. Preferably present at a level of from 0.015 to 50%, more preferably from 5% to 30%, more preferably from 8% to 25%, most preferably from 12% to 205 by weight of the composition.

The phosphate-containing builder material preferably comprises tetrasodium pyrophosphate or even more preferably anhydrous sodium tripolyphosphate.

Suitable water-soluble builder compounds include the water soluble monomeric polycarboxylates, or their acid forms, homo or copolymeric polycarboxylic acids or their salts in which the polycarboxylic acid comprises at least two carboxylic radicals separated from each other by not more that two carbon atoms, borates, and mixtures of any of the foregoing.

The carboxylate or polycarboxylate builder can be momomeric or oligomeric in type although monomeric polycarboxylates are generally preferred for reasons of cost and performance.

Suitable carboxylates containing one carboxy group include the water soluble salts of lactic acid, glycolic acid and ether derivatives thereof. Polycarboxylates containing two carboxy groups include the water-soluble salts of succinic acid, malonic acid, (ethylenedioxy)diacetic acid, maleic acid, diglycolic acid, tartaric acid, tartronic acid and fumaric acid, as well as the ether carboxylates and the sulfinyl carboxylates. Polycarboxylates or their acids containing three carboxy groups include, in particular, water-soluble citrates, aconitrates and citraconates as well as succinate derivatives such as the carboxymethyloxysuccinates described in British Patent No. 1,379,241, lactoxysuccinates described in British Patent No. 1,389,732, and aminosuccinates described in Netherlands Application 7205873, and the oxypolycarboxylate materials such as 2-oxa-1,1,3-propane tricarboxylates described in British Patent No. 1,387,447. The most preferred polycarboxylic acid containing three carboxy groups is citric acid, preferably present a t a level of from 0.1% to 15%, more preferably from 0.5% to 8% by weight of the composition.

Polycarboxylates containing four carboxy groups include oxydisuccinates disclosed in British Patent No. 1,261,829, 1,1,2,2-ethane tetracarboxylates, 1,1,3,3-propane tetracarboxylates and 1,1,2,3-propane tetracarboxylates. Polycarboxylates containing sulfo substituents include the sulfosuccinate derivatives disclosed in British Patent Nos. 1,398,421 and 1,398,422 and in U.S. Pat. No. 3,936,448, and the sulfonated pyrolysed citrates described in British Patent No. 1,439,000. Preferred polycarboxylates are hydroxycarboxylates containing up to three carboxy groups per molecule, more particularly citrates.

The parent acids of the monomeric or oligomeric polycarboxylate chelating agents or mixtures thereof with their salts, e.g. citric acid or citrate/citric acid mixtures are also contemplated as useful builder components.

Borate builders, as well as builders containing borate-forming materials that can produce borate under detergent storage or wash conditions are useful water-soluble builders herein.

Suitable examples of water-soluble phosphate builders are the alkali metal tripolyphosphates, sodium, potassium and ammonium pyrophosphate, sodium and potassium and ammonium pyrophosphate, sodium and potassium orthophosphate, sodium polymeta/phosphate in which the degree of polymerization ranges from about 6 to 21, and salts of phytic acid.

Partially Soluble or Insoluble Builder Compound

The detergent compositions or compositions thereof in accord with the present invention may contain a partially soluble or insoluble builder compound, typically present in detergent compositions at a level of from 1% to 80% by weight, preferably from 10% to 70% by weight, most preferably from 20% to 60% weight of the composition.

Examples of largely water insoluble builders include the sodium aluminosilicates.

Suitable aluminosilicate zeolites have the unit cell formula Na_(z)[(AlO₂)_(z)(SiO₂)y]. xH₂O wherein z and y are at least 6; the molar ratio of z to y is from 1.0 to 0.5 and x is at least 5, preferably from 7.5 to 276, more preferably from 10 to 264. The aluminosilicate material are in hydrated form and are preferably crystalline, containing from 10% to 28%, more preferably from 18% to 22% water in bound form.

The aluminosilicate zeolites can be naturally occurring materials, but are preferably synthetically derived. Synthetic crystalline aluminosilicate ion exchange materials are available under the designations Zeolite A, Zeolite B, Zeolite P, Zeolite X, Zeolite HS and mixtures thereof. Zeolite A has the formula:

Na₁₂[AlO₂)₁₂(SiO₂)₁₂].xH₂O

wherein x is from 20 to 30, especially 27. Zeolite X has the formula Na₈₆[(AlO₂)₈₆(SiO₂)₁₀₆].276H₂O.

Another preferred aluminosilicate zeolite is zeolite MAP builder. The zeolite MAP can be present at a level of from 1% to 80%, more preferably from 15% to 40% by weight of the compositions.

Zeolite MAP is described in EP 384070A (Unilever). It is defined as an alkali metal alumino-silicate of the zeolite P type having a silicon to aluminium ratio not greater than 1.33, preferably within the range from 0.9 to 1.33 and more preferably within the range of from 0.9 to 1.2.

Of particular interest is zeolite MAP having a silicon to aluminium ratio not greater than 1.15 and, more particularly, not greater than 1.07.

In a preferred aspect the zeolite MAP detergent builder has a particle size, expressed as a d₅₀ value of from 1.0 to 10.0 micrometers, more preferably from 2.0 to 7.0 micrometers, most preferably from 2.5 to 5.0 micrometers.

The d_(5O) value indicates that 50% by weight of the particles have a diameter smaller than that figure. The particle size may, in particular be determined by conventional analytical techniques such as microscopic determination using a scanning electron microscope or by means of a laser granulometer. Other methods of establishing d₅₀ values are disclosed in EP 384070A.

Enzyme

Another preferred ingredient useful in the detergent compositions or components thereof is one or more additional enzymes.

Preferred additional enzymatic materials include the commercially available lipases, cutinases, amylases, neutral and alkaline proteases, cellulases, endolases, esterases, pectinases, lactases and peroxidases conventionally incorporated into detergent compositions. Suitable enzymes are discussed in U.S. Pat. Nos. 3,519,570 and 3,533,139.

Preferred commercially available protease enzymes include those sold under the tradenames Alcalase, Savinase, Primase, Durazym, and Esperase by Novo Industries A/S (Denmark), those sold under the tradename Maxatase, Maxacal and Maxapem by Gist-Brocades, those sold by Genencor International, and those sold under the tradename Opticlean and Optimase by Solvay Enzymes. Protease enzyme may be incorporated into the compositions in accordance with the invention at a level of from 0.0001% to 4% active enzyme by weight of the composition.

Preferred amylases include, for example, α-amylases obtained from a special strain of B licheniformis, described in more detail in GB-1,269,839 (Novo). Preferred commercially available amylases include for example, those sold under the tradename Rapidase by Gist-Brocades, and those sold under the tradename Termamyl and BAN by Novo Industries A/S. Amylase enzyme may be incorporated into the composition in accordance with the invention at a level of from 0.0001% to 2% active enzyme by weight of the composition.

Lipolytic enzyme may be present at levels of active lipolytic enzyme of from 0.0001% to 2% by weight, preferably 0.001% to 1% by weight, most preferably from 0.001% to 0.5% by weight of the compositions.

The lipase may be fungal or bacterial in origin being obtained, for example, from a lipase producing strain of Humicola sp., Thermomyces sp. or Pseudomonas sp. including Pseudomonas pseudoalcaligenes or Pseudomas fluorescens. Lipase from chemically or genetically modified mutants of these strains are also useful herein. A preferred lipase is derived from Pseudomonas pseudoalcalienes, which is described in Granted European Patent, EP-B-0218272.

Another preferred lipase herein is obtained by cloning the gene from Humicola lanuginosa and expressing the gene in Aspergillus oryza, as host, as described in European Patent Application, EP-A-0258 068, which is commercially available from Novo Industri A/S, Bagsvaerd, Denmark, under the trade name Lipolase. This lipase is also described in U.S. Pat. No. 4,810,414, Huge-Jensen et al, issued Mar. 7, 1989.

Organic Polymeric Compound

Organic polymeric compounds are preferred additional components of the detergent compositions or components thereof in accord with the invention, and are preferably present as components of any particulate components where they may act such as to bind the particulate component together. By organic polymeric compound it is meant herein essentially any polymeric organic compound commonly used as dispersants, and anti-redeposition and soil suspension agents in detergent compositions, including any of the high molecular weight organic polymeric compounds described as clay flocculating agents herein, not being an quatemised ethoxylated (poly)amine clay-soil removal/anti-redeposition agent in accord with the invention.

Organic polymeric compound is typically incorporated in the detergent compositions of the invention at a level of from 0.1% to 30%, preferably from 0.5% to 15%, most preferably from 1% to 10% by weight of the compositions.

Examples of organic polymeric compounds include the water soluble organic homo- or co-polymeric polycarboxylic acids or their salts in which the polycarboxylic acid comprises at least two carboxyl radicals separated from each other by not more than two carbon atoms. Polymers of the latter type are disclosed in GB-A-1,596,756.

Examples of such salts are polyacrylates of MWt 1000-5000 and their copolymers with maleic anhydride, such copolymers having a molecular weight of from 2000 to 100,000, especially 40,000 to 80,000.

The polyamino compounds are useful herein including those derived from aspartic acid such as those disclosed in EP-A-305282, EP-A-305283 and EP-A-351629.

Terpolymers containing monomer units selected from maleic acid, acrylic acid, polyaspartic acid and vinyl alcohol, particularly those having an average molecular weight of from 5,000 to 10,000, are also suitable herein.

Other organic polymeric compounds suitable for incorporation in the detergent compositions herein include cellulose derivatives such as methylcellulose, carboxymethylcellulose, hydroxypropylmethylcellulose and hydroxyethylcellulose.

Further useful organic polymeric compounds are the polyethylene glycols, particularly those of molecular weight 1000-10000, more particularly 2000 to 8000 and most preferably about 4000.

Suds Suppressing System

The detergent compositions of the invention, when formulated for use in machine washing compositions, preferably comprise a suds suppressing system present at a level of from 0.01% to 15%, preferably from 0.05% to 10%, most preferably from 0.1% to 5% by weight of the composition.

Suitable suds suppressing systems for use herein may comprise essentially any known antifoam compound, including, for example silicone antifoam compounds and 2-alkyl alcanol antifoam compounds.

By antifoam compound it is meant herein any compound or mixtures of compounds which act such as to depress the foaming or sudsing produced by a solution of a detergent composition, particularly in the presence of agitation of that solution.

Particularly preferred antifoam compounds for use herein are silicone antifoam compounds defined herein as any antifoam compound including a silicone component. Such silicone antifoam compounds also typically contain a silica component. The term “silicone” as used herein, and in general throughout the industry, encompasses a variety of relatively high molecular weight polymers containing siloxane units and hydrocarbyl group of various types. Preferred silicone antifoam compounds are the siloxanes, particularly the polydimethylsiloxanes having trimethylsilyl end blocking units.

Other suitable antifoam compounds include the monocarboxylic fatty acids and soluble salts thereof. These materials are described in U.S. Pat. No. 2,954,347, issued Sep. 27, 1960 to Wayne St. John. The monocarboxylic fatty acids, and salts thereof, for use as suds suppressor typically have hydrocarbyl chains of 10 to 24 carbon atoms, preferably 12 to 18 carbon atoms. Suitable salts include the alkali metal salts such as sodium, potassium, and lithium salts, and ammonium and alkanolammonium salts.

Other suitable antifoam compounds include, for example, high molecular weight fatty esters (e.g. fatty acid triglycerides), fatty acid esters of monovalent alcohols, aliphatic C₁₈-C₄₀ ketones (e.g. stearone) N-alkylated amino triazines such as tri- to hexa-alkylmelamines or di- to tetra alkyldiamine chlortriazines formed as products of cyanuric chloride with two or three moles of a primary or secondary amine containing 1 to 24 carbon atoms, propylene oxide, bis stearic acid amide and monostearyl di-alkali metal (e.g. sodium, potassium, lithium) phosphates and phosphate esters.

A preferred suds suppressing system comprises:

(a) antifoam compound, preferably silicone antifoam compound, most preferably a silicone antifoam compound comprising in combination

(i) polydimethyl siloxane, at a level of from 50% to 99%, preferably 75% to 95% by weight of the silicone antifoam compound; and

(ii) silica, at a level of from 1% to 50%, preferably 5% to 25% by weight of the silicone/silica antifoam compound;

 wherein said silica/silicone antifoam compound is incorporated at a level of from 5% to 50%, preferably 10% to 40% by weight;

(b) a dispersant compound, most preferably comprising a silicone glycol rake copolymer with a polyoxyalkylene content of 72-78% and an ethylene oxide to propylene oxide ratio of from 1:0.9 to 1:1.1, at a level of from 0.5% to 10%, preferably 1% to 10% by weight; a particularly preferred silicone glycol rake copolymer of this type is DCO544, commercially available from DOW Coming under the tradename DCO544;

(c) an inert carrier fluid compound, most preferably comprising a C₁₆-C₁₈ ethoxylated alcohol with a degree of ethoxylation of from 5 to 50, preferably 8 to 15, at a level of from 5% to 80%, preferably 10% to 70%, by weight;

A highly preferred particulate suds suppressing system is described in EP-A-0210731 and comprises a silicone antifoam compound and an organic carrier material having a melting point in the range 50° C. to 85° C., wherein the organic carrier material comprises a monoester of glycerol and a fatty acid having a carbon chain containing from 12 to 20 carbon atoms. EP-A-0210721 discloses other preferred particulate suds suppressing systems wherein the organic carrier material is a fatty acid or alcohol having a carbon chain containing from 12 to 20 carbon atoms, or a mixture thereof, with a melting point of from 45° C. to 80° C.

Polymeric Dye Transfer Inhibiting Agents

The detergent compositions herein may also comprise from 0.01% to 10%, preferably from 0.05% to 0.5% by weight of polymeric dye transfer inhibiting agents.

The polymeric dye transfer inhibiting agents are preferably selected from polyamine N-oxide polymers, copolymers of N-vinylpyrrolidone and N-vinylimidazole, polyvinylpyrrolidonepolymers or combinations thereof, whereby these polymers can be cross-linked polymers.

a) Polyamine N-Oxide Polymers

Polyamine N-oxide polymers suitable for use herein contain units having the following structure formula:

wherein P is a polymerisable unit, and

R are aliphatic, ethoxylated aliphatics, aromatic, heterocyclic or alicyclic groups or any combination thereof whereto the nitrogen of the N—O group can be attached or wherein the nitrogen of the N—O group is part of these groups.

The N—O group can be represented by the following general structures

wherein R1, R2, and R3 are aliphatic groups, aromatic, heterocyclic or alicyclic groups or combinations thereof, x or/and y or/and z is 0 or 1 and wherein the nitrogen of the N—O group can be attached or wherein the nitrogen of the N—O group forms part of these groups. The N—O group can be part of the polymerisable unit (P) or can be attached to the polymeric backbone or a combination of both.

Suitable polyamine N-oxides wherein the N—O group forms part of the polymerisable unit comprise polyamine N-oxides wherein R is selected from aliphatic, aromatic, alicyclic or heterocyclic groups. One class of said polyamine N-oxides comprises the group of polyamine N-oxides wherein the nitrogen of the N—O group forms part of the R-group. Preferred polyamine N-oxides are those wherein R is a heterocyclic group such as pyrridine, pyrrole, imidazole, pyrrolidine, piperidine, quinoline, acridine and derivatives thereof.

Other suitable polyamine N-oxides are the polyamine oxides whereto the N—O group is attached to the polymerisable unit. A preferred class of these polyamine N-oxides comprises the polyamine N-oxides having the general formula (I) wherein R is an aromatic,heterocyclic or alicyclic groups wherein the nitrogen of the N—O functional group is part of said R group. Examples of these classes are polyamine oxides wherein R is a heterocyclic compound such as pyrridine, pyrrole, imidazole and derivatives thereof.

The polyamine N-oxides can be obtained in almost any degree of polymerisation. The degree of polymerisation is not critical provided the material has the desired water-solubility and dye-suspending power. Typically, the average molecular weight is within the range of 500 to 1000,000.

b) Copolymers of N-Vinylpyrrolidone and N-Vinylimidazole

Suitable herein are coploymers of N-vinylimidazole and N-vinylpyrrolidone having an average molecular weight range of from 5,000 to 50,000. The preferred copolymers have a molar ratio of N-vinylimidazole to N-vinylpyrrolidone from 1 to 0.2.

c) Polyvinylpyrrolidone

The detergent compositions herein may also utilize polyvinylpyrrolidone (“PVP”) having an average molecular weight of from 2,500 to 400,000. Suitable polyvinylpyrrolidones are commercially available from ISP Corporation, New York, N.Y. and Montreal, Canada under the product names PVP K-15 (viscosity molecular weight of 10,000), PVP K-30 (average molecular weight of 40,000), PVP K-60 (average molecular weight of 160,000), and PVP K-90 (average molecular weight of 360,000). PVP K-15 is also available from ISP Corporation. Other suitable polyvinylpyrrolidones which are commercially available from BASF Cooperation include Sokalan HP 165 and Sokalan HP 12.

d) Polyvinyloxazolidone

The detergent compositions herein may also utilize polyvinyloxazolidones as polymeric dye transfer inhibiting agents. Said polyvinyloxazolidones have an average molecular weight of from 2,500 to 400,000.

e) Polyvinylimidazole

The detergent compositions herein may also utilize polyvinylimidazole as polymeric dye transfer inhibiting agent. Said polyvinylimidazoles preferably have an average molecular weight of from 2,500 to 400,000.

Optical Brightener

The detergent compositions herein also optionally contain from about 0.005% to 5% by weight of certain types of hydrophilic optical brighteners.

Hydrophilic optical brighteners useful herein include those having the structural formula:

wherein R¹ is selected from anilino, N-2-bis-bydroxyethyl and NH-2-hydroxyethyl; R₂ is selected from N-2-bis-hydroxyethyl, N-2-hydroxyethyl-N-methylamino, morphilino, chloro and amino; and M is a salt-forming cation such as sodium or potassium.

When in the above formula, R₁ is anilino, R₂ is N-2-bis-hydroxyethyl and M is a cation such as sodium, the brightener is 4,4′,-bis[(4-anilino-6-(N-2-bis-hydroxyethyl)-s-triazine-2-yl)amino]-2,2′-stilbenedisulfonic acid and disodium salt. This particular brightener species is commercially marketed under the tradename Tinopal-UNPA-GX by Ciba-Geigy Corporation. Tinopal-UTNPA-GX is the preferred hydrophilic optical brightener useful in the detergent compositions herein.

When in the above formula, R₁ is anilino, R₂ is N-2-hydroxyethyl-N-2-methylamino and M is a cation such as sodium, the brightener is 4,4′-bis[(4-anilino-6-(N-2-hydroxyethyl-N-methylamino)-s-triazine-2-yl)amino]2,2′-stilbenedisulfonic acid disodium salt. This particular brightener species is commercially marketed under the tradename Tinopal 5BM-GX by Ciba-Geigy Corporation.

When in the above formula, R₁ is anilino, R₂ is morphilino and M is a cation such as sodium, the brightener is 4,4′-bis[(4-anilino-6-morphilino-s-triazine-2-yl)amino]_(2,2)′-stilbenedisulfonic acid, sodium salt. This particular brightener species is commercially marketed under the tradename Tinopal AMS-GX by Ciba Geigy Corporation.

Polymeric Soil Release Agent

Known polymeric soil release agents, hereinafter “SRA”, can optionally be employed in the present detergent compositions. If utilized, SRA's will generally comprise from 0.01% to 10.0%, typically from 0.1% to 5%, preferably from 0.2% to 3.0% by weight, of the compositions.

Preferred SRA's typically have hydrophilic segments to hydrophilize the surface of hydrophobic fibers such as polyester and nylon, and hydrophobic segments to deposit upon hydrophobic fibers and remain adhered thereto through completion of washing and rinsing cycles, thereby serving as an anchor for the hydrophilic segments. This can enable stains occurring subsequent to treatment with the SRA to be more easily cleaned in later washing procedures.

Preferred SRA's include oligomeric terephthalate esters, typically prepared by processes involving at least one transesterification/oligomerization, often with a metal catalyst such as a titanium(IV) alkoxide. Such esters may be made using additional monomers capable of being incorporated into the ester structure through one, two, three, four or more positions, without, of course, forming a densely crosslinked overall structure.

Suitable SRA's include a sulfonated product of a substantially linear ester oligomer comprised of an oligomeric ester backbone of terephthaloyl and oxyalkyleneoxy repeat units and allyl-derived sulfonated terminal moieties covalently attached to the backbone, for example as described in U.S. Pat. No. 4,968,451, Nov. 6, 1990 to J. J. Scheibel and E. P. Gosselink. Such ester oligomers can be prepared by: (a) ethoxylating allyl alcohol; (b) reacting the product of (a) with dimethyl terephthalate (“DMT”) and 1,2-propylene glycol (“PG”) in a two-stage transesterification/oligomerization procedure; and (c) reacting the product of (b) with sodium metabisulfite in water. Other SRA's include the nonionic end-capped 1,2-propylene/polyoxyethylene terephthalate polyesters of U.S. Pat. No. 4,711,730, Dec. 8, 1987 to Gosselink et al., for example those produced by transesterification/oligomerization of poly(ethyleneglycol)methyl ether, DMT, PG and poly(ethyleneglycol) (“PEG”). Other examples of SKA's include: the partly- and fully-anionic-end-capped oligomeric esters of U.S. Pat. No. 4,721,580, Jan. 26, 1988 to Gosselink, such as oligomers from ethylene glycol (“EG”), PG, DMT and Na-3,6-dioxa-8-hydroxyoctanesulfonate; the nonionic-capped block polyester oligomeric compounds of U.S. Pat. No. 4,702,857, Oct. 27, 1987 to Gosselink, for example produced from DMT, methyl (Me)-capped PEG and EG and/or PG, or a combination of DMT, EG and/or PG, Me-capped PEG and Na-dimethyl-5-sulfoisophthalate; and the anionic, especially sulfoaroyl, end-capped terephthalate esters of U.S. Pat. No. 4,877,896, Oct. 31, 1989 to Maldonado, Gosselink et al., the latter being typical of SRA's useful in both laundry and fabric conditioning products, an example being an ester composition made from m-sulfobenzoic acid monosodium salt, PG and DMT, optionally but preferably further comprising added PEG, e.g., PEG 3400.

SRA's also include: simple copolymeric blocks of ethylene terephthalate or propylene terephthalate with polyethylene oxide or polypropylene oxide terephthalate, see U.S. Pat. No. 3,959,230 to Hays, May 25, 1976 and U.S. Pat. No. 3,893,929 to Basadur, Jul. 8, 1975; cellulosic derivatives such as the hydroxyether cellulosic polymers available as METHOCEL from Dow; the C₁-C₄ alkyl celluloses and C₄ hydroxyalkyl celluloses, see U.S. Pat. No. 4,000,093, Dec. 28, 1976 to Nicol, et al.; and the methyl cellulose ethers having an average degree of substitution (methyl) per anhydroglucose unit from about 1.6 to about 2.3 and a solution viscosity of from about 80 to about 120 centipoise measured at 20° C. as a 2% aqueous solution. Such materials are available as METOLOSE SM100 and METOLOSE SM200, which are the trade names of methyl cellulose ethers manufactured by Shin-etsu Kagaku Kogyo KK.

Additional classes of SRA's include: (I) nonionic terephthalates using diisocyanate coupling agents to link polymeric ester structures, see U.S. Pat. No. 4,201,824, Violland et al. and U.S. Pat. No. 4,240,918 Lagasse et al.; and (II) SRA's with carboxylate terminal groups made by adding trimellitic anhydride to known SRA's to convert terminal hydroxyl groups to trimellitate esters. With the proper selection of catalyst, the trimellitic anhydride forms linkages to the terminals of the polymer through an ester of the isolated carboxylic acid of trimellitic anhydride rather than by opening of the anhydride linkage. Either nonionic or anionic SRA's may be used as starting materials as long as they have hydroxyl terminal groups which may be esterified. See U.S. Pat. No. 4,525,524 Tung et al. Other classes include: (III) anionic terephthalate-based SRA's of the urethane-linked variety, see U.S. Pat. No. 4,201,824, Violland et al.;

Other Optional Ingredients

Other optional ingredients suitable for inclusion in the compositions of the invention include colours and filler salts, with sodium sulfate being a preferred filler salt.

Highly preferred compositions preferably contain from about 2% to about 10% by weight of an organic citric acid, preferably citric acid. Also preferably in combination with a carbonate salt, minor amounts (e.g., less than about 20% by weight) of neutralizing agents, buffering agents, phase regulants, hydrotropes, enzyme stabilizing agents, polyacids, suds regulants, opacifiers, anti-oxidants, bactericides, dyes, perfumes, such as those described in U.S. Pat. No. 4,285,841 to Barrat et al., issued Aug. 25, 1981 (herein incorporated by reference), can be present in the compositions.

Form of the Compositions

The detergent component of the invention can be made via a variety of methods, including dry-mixing and agglomerating of the various compounds comprised in the detergent component.

The detergent component preferably forms part of a detergent composition. The compositions in accordance with the invention can take a variety of physical forms including liquid and solid forms such as tablet, flake, pastille and bar, and preferably granular forms.

The compositions in accord with the present invention can also be used in or in combination with bleach additive compositions, for example comprising chlorine bleach, as mentioned above.

However, since preferred detergent compositions of the invention are solid, most liquid chlorine-based bleaching will not be suitable for these detergent compositions and only granular or powder chlorine-based bleaches will be suitable.

Alternatively, the detergent compositions can be formulated such that they are chlorine-based bleach-compatible, thus ensuring that a chlorine based bleach can be added to the detergent composition by the user at the beginning or during the washing process.

The chlorine-based bleach is such that a hypochlorite species is formed in aqueous solution. The hypochlorite ion is chemically represented by the formula OCI⁻.

Those bleaching agents which yield a hypochlorite species in aqueous solution include alkali metal and alkaline earth metal hypochlorites, hyposchlorite addition products, chloramines, chlorimines, chloramides, and chlorimides. Specific examples of compounds of this type include sodium hypochlorite, potassium hypochlorite, monobasic calcium hypochlorite, dibasic magnesium hypochlorite, chlorinated trisodium phosphate dodecahydrate, potassium dichloroisocyanurate, sodium dichloroisocyanurate sodium dichloroisocyanurate dihydrate, trichlorocyanuric acid, 1,3-dichloro-5,5-dimethylhydantoin, N-chlorosulfamide, Chloramine T, Dichloramine T, chloramine B and Dichloramine B. A preferred bleaching agent for use in the compositions of the instant invention is sodium hypochlorite, potassium hypochlorite, or a mixture thereof. A preferred chlorine-based bleach can be Triclosan (trade name).

Most of the above-described hypochlorite-yielding bleaching agents are available in solid or concentrated form and are dissolved in water during preparation of the compositions of the instant invention. Some of the above materials are available as aqueous solutions.

In general, granular detergent compositions in accordance with the present invention can be made via a variety of methods including dry mixing, spray drying, agglomeration and granulation. The quaternised clay-soil removal/anti-redeposition agent in accord with the present invention can be added to the other detergent components by dry-mixing, agglomeration (preferably combined with a carrier material) or as a spray-dried component.

The mean particle size of the components of granular compositions in accordance with the invention, should preferably be such that no more that 25% of the particles are greater than 1.8 mm in diameter and not more than 25% of the particles are less than 0.25 mm in diameter. Preferably the mean particle size is such that from 10% to 50% of the particles has a particle size of from 0.2 mm to 0.7 mm in diameter.

The term mean particle size as defined herein is calculated by sieving a sample of the composition into a number of fractions (typically 5 fractions) on a series of sieves, preferably Tyler sieves. The weight fractions thereby obtained are plotted against the aperture size of the sieves. The mean particle size is taken to be the aperture size through which 50% by weight of the sample would pass.

The bulk density of granular detergent compositions in accordance with the present invention typically have a bulk density of at least 200 g/liter, more preferably from 300 g/liter to 1200 g/liter, more preferably from 300 g/liter to 800 gr/liter, most preferably from 330 g/liter to 600 gr/liter. Bulk density is measured by means of a simple funnel and cup device consisting of a conical funnel moulded rigidly on a base and provided with a flap valve at its lower extremity to allow the contents of the funnel to be emptied into an axially aligned cylindrical cup disposed below the funnel. The funnel is 130 mm high and has internal diameters of 130 mm and 40 mm at its respective upper and lower extremities. It is mounted so that the lower extremity is 140 mm above the upper surface of the base. The cup has an overall height of 90 mm, an internal height of 87 mm and an internal diameter of 84 mm. Its nominal volume is 500 ml.

To carry out a measurement, the funnel is filled with powder by hand pouring, the flap valve is opened and powder allowed to overfill the cup. The filled cup is removed from the frame and excess powder removed from the cup by passing a straight edged implement eg; a knife, across its upper edge. The filled cup is then weighed and the value obtained for the weight of powder doubled to provide a bulk density in g/liter. Replicate measurements are made as required.

Laundry Washing Method

Machine laundry methods herein typically comprise treating soiled laundry with an aqueous wash solution in a washing machine having dissolved or dispensed therein an effective amount of a machine laundry detergent composition in accord with the invention. By an effective amount of the detergent composition it is meant from 10 g to 300 g of product dissolved or dispersed in a wash solution of volume from 5 to 65 liters, as are typical product dosages and wash solution volumes commonly employed in conventional machine laundry methods.

In a preferred use aspect the detergent composition is formulated such that it is suitable for hand washing.

In another preferred aspect the detergent composition is a pre-treatment or soaking composition, to be used to pre-treat or soak soiled and stained fabrics.

Abbreviations Used in Examples

In the detergent compositions, the abbreviated component identifications have the following meanings:

LAS Sodium linear C₁₁₋₁₃ alkyl benzene sulfonate TAS Sodium tallow alkyl sulfate CxyAS Sodium C_(1x)-C_(1y) alkyl sulfate C46SAS Sodium C₁₄-C₁₆ secondary (2,3) alkyl sulfate CxyEzS Sodium C_(1x)-C_(1y) alkyl sulfate condensed with z moles of ethylene oxide CxyEz C_(1x)-C_(1y) predominantly linear primary alcohol condensed with an average of z moles of ethylene oxide QAS R₂.N⁺(CH₃)₂(C₂H₄OH) with R₂ = C₁₂-C₁₄ QAS 1 R₂.N⁺(CH₃)₂(C₂H₄OH) with R₂ = C₈-C₁₁ SADS Sodium C₁₄-C₂₂ alkyl disulfate of formula 2-(R).C₄ H₇.-1,4-(SO₄—)₂ where R = C₁₀-C₁₈ SADE2S Sodium C₁₄-C₂₂ alkyl disulfate of formula 2-(R).C₄ H₇.-1,4-(SO₄—)₂ where R = C₁₀-C₁₈, condensed with z moles of ethylene oxide MES x-sulpho methylaster of C₁₈ fatty acid APA C₈-C₁₀ amido propyl dimethyl amine Soap Sodium linear alkyl carboxylate derived from an 80/20 mixture of tallow and coconut fatty acids STS Sodium toluene sulphonate CFAA C₁₂-C₁₄ (coco) alkyl N-methyl glucamide TFAA C₁₆-C₁₈ alkyl N-methyl glucamide TPKFA C₁₂-C₁₄ topped whole cut fatty acids STPP Anhydrous sodium tripolyphosphate TSPP Tetrasodium pyrophosphate Zeolite A Hydrated sodium aluminosilicate of formula Na₁₂(AlO₂SiO₂)₁₂.27H₂O having a primary particle size in the range from 0.1 to 10 micrometers (weight expressed on an anhydrous basis) NaSKS-6 Crystalline layered silicate of formula δ-Na₂Si₂O₅ Citric acid Anhydrous citric acid Borate Sodium borate Carbonate Anydrous sodium carbonate with a particle size between 200 μm and 900 μm Bicarbonate Anhydrous sodium bicarbonate with a particle size distribution between 400 μm and 1200 μm Silicate Amorphous sodium silicate (SiO₂:Na₂O = 2.0:1) Sulfate Anhydrous sodium sulfate Mg sulfate Anhydrous magnesium sulfate Citrate Tri-sodium citrate dihydrate of activity 86.4% with a particle size distribution between 425 μm and 850 μm MA/AA Copolymer of 1:4 maleic/acrylic acid, average molecular weight about 70,000 MA/AA (1) Copolymer of 4:6 maleic/acrylic acid, average molecular weight about 10,000 AA Sodium polyacrylate polymer of average molecular weight 4,500 CMC Sodium carboxymethyl cellulose Cellulose Methyl cellulose ether with a degree of ether polymerization of 650 available from Shin Etsu Chemicals Protease Proteolytic enzyme, having 3.3% by weight of active enzyme, sold by NOVO Industries A/S under the tradename Savinase Protease I Proteolytic enzyme, having 4% by weight of active enzyme, as described in WO 95/10591, sold by Genencor Int. Inc. Alcalase Proteolytic enzyme, having 5.3% by weight of active enzyme, sold by NOVO Industries A/S Cellulase Cellulytic enzyme, having 0.23% by weight of active enzyme, sold by NOVO Industries A/S under the tradename Carezyme Amylase Amylolytic enzyme, having 1.6% by weight of active enzyme, sold by NOVO Industries A/S under the tradename Termarnyl 120T Lipase Lipolytic enzyme, having 2.0% by weight of active enzyme, sold by NOVO Industries A/S under the tradename Lipolase Lipase (1) Lipolytic enzyme, having 2.0% by weight of active enzyme, sold by NOVO Industries A/S under the tradename Lipolase Ultra Endolase Endoglucanase enzyme, having 1.5% by weight of active enzyme, sold by NOVO Industries A/S PB4 Sodium perborate tetrahydrate of nominal formula NaBO₂.3H₂O.H₂O₂ PB1 Anhydrous sodium perborate bleach of nominal formula NaBO₂.H₂O₂ Percarbonate Sodium percarbonate of nominal formula 2Na₂CO₃.3H₂O₂ DOBS Decanoyl oxybenzene sulfonate in the form of the sodium salt DPDA Diperoxydodecanedioc acid NOBS Nonanoyloxybenzene sulfonate in the form of the sodium salt NAC-OBS (6-nonamidocaproyl) oxybenzene sulfonate TAED Tetraacetylethylenediamine DTPA Diethylene triamine pentaacetic acid DTPMP Diethylene triamine penta (methylene phosphonate), marketed by Monsanto under the Tradename Dequest 2060 EDDS Ethylenediamine-N,N′-disuccinic acid, (S,S) isomer in the form of its sodium salt. Photo- Sulfonated zinc phthlocyanine encapsulated in bleach activated (1) dextrin soluble polymer Photo- Sulfonated alumino phthlocyanine encapsulated in activated bleach (2) dextrin soluble polymer Brightener 1 Disodium 4,4′-bis(2-sulphostyryl)biphenyl Brightener 2 Disodium 4,4′-bis(4-anilino-6-morpholino-1.3.5- triazin-2-yl)amino) stilbene-2:2′-disulfonate HEDP 1,1-hydroxyethane diphosphonic acid PEGx Polyethylene glycol, with a molecular weight of x (typically 4,000) PEO Polyethylene oxide, with an average molecular weight of 50,000 TEPAE Tetraethylenepentaamine ethoxylate PVI Polyvinyl imidosole, with an average molecular weight of 20,000 PVP Polyvinylpyrolidone polymer, with an average molecular weight of 60,000 PVNO Polyvinylpyridine N-oxide polymer, with an average molecular weight of 50,000 PVPVI Copolymer of polyvinylpyrolidone and vinylimidazole, with an average molecular weight of 20,000 QEA bis((C₂H₅O)(C₂H₄O)_(n))(CH₃)—N⁺—C₆H₁₂—N⁺—(CH₃) bis((C₂H₅O)—(C₂H₄O))_(n), wherein n = from 20 to 30 SRP 1 Anionically end capped poly esters SRP 2 Diethoxylated poly (1,2 propylene terephtalate) short block polymer PEI Polyethyleneimine with an average molecular weight of 1800 and an average ethoxylation degree of 7 ethyleneoxy residues per nitrogen Silicone Polydimethylsiloxane foam controller with siloxane- antifoam oxyalkylene copolymer as dispersing agent with a ratio of said foam controller to said dispersing agent of 10:1 to 100:1 Opacifier Water based monostyrene latex mixture, sold by BASF Aktiengesellschaft under the tradename Lytron 621 Wax Paraffin wax

In the following examples all levels are quoted as % by weight of the composition:

EXAMPLE 1

The following laundry detergent compositions A to F are in accord with the invention:

A B C D E F LAS 8.0 8.0 8.0 2.0 6.0 6.0 TAS — 0.5 — 0.5 1.0 0.1 C46AS 2.0 2.5 — — — — C25AS — — — 7.0 4.5 5.5 SADS — — 1.0 2.0 — — MES — 5.0 2.0 — — — C25E5 — — 3.4 10.0  4.6 4.6 C25E7 3.4 3.4 1.0 — — — C25E11S 2.0 — — — 5.0 4.5 QAS — 0.8 — — — — QAS(I) — — — 0.8 0.5 1.0 Zeolite A — — — 18.1  20.0  18.1  STPP 20.0  22.0  30.0  — — — Citric acid — — — 2.5 — 2.5 Carbonate 13.0  13.0  27.0  10.0  10.0  13.0  SKS-6 — — — 10.  — 10.0  Silicate 1.4 1.4 3.0 0.3 0.5 0.3 Citrate — 1.0 — 3.0 — — Sulfate 26.1  26.1  26.1  6.0 — — Mg sulfate 0.3 — — 0.2 — 0.2 MA/AA 0.3 0.3 0.3 4.0 1.0 1.0 CMC 0.2 0.2 0.2 0.2 0.4 0.4 PB4 9.0 9.0 5.0 — — — Percarbonate — — — — 18.0  18.0  NAC-OBS 1.5 0.4 — — — 4.2 NOBS — 2.0 1.0 4.0 2.0 — DOBS 2.0 — — — 2.0 — DTPMP  0.25  0.25  0.25  0.25 — — SRPI — — — 0.2 — 0.2 EDDS —  0.25 0.4 — 0.5 0.5 CFAA — 1.0 — 2.0 — — HEDP 0.3 0.3 0.3 0.3 0.4 0.4 QEA — — — 0.2 — 0.5 Protease I — —  0.26 1.0 — — Protease  0.26  0.26 — — 1.5 1.0 Cellulase 0.3 — — 0.3 0.3 0.3 Amylase 0.1 0.1 0.1 0.4 0.5 0.5 Lipase (I) 0.3 — — 0.5 0.5 0.5 Photoactivated 15 ppm 15 ppm 15 ppm — 20 ppm 20 ppm bleach (ppm) PVNO/PVPVI — — — 0.1 — — Brightener 1  0.09  0.09  0.09 —  0.09  0.09 Perfume 0.3 0.3 0.3 0.4 0.4 0.4 Silicone 0.5 0.5 0.5 — 0.3 0.3 antifoam Misc/minors to 100% Density in 700    700    700    750    750    750    g/litre

EXAMPLE 2

The following detergent formulations are in accord with the invention.

G H I J Blown powder MES 2.0 0.5 1.0 — SADS — — — 2.0 LAS 6.0 5.0 11.0  6.0 TAS 2.0 — — 2.0 Zeolite A 24.0  — — 20.0  STPP — 27.0  24.0  — Sulfate 4.0 6.0 13.0  — MA/AA 1.0 4.0 6.0 2.0 Silicate 1.0 7.0 3.0 3.0 CMC 1.0 1.0 0.5 0.6 Brightener 1 0.2 0.2 0.2 0.2 Silicone antifoam 1.0 1.0 1.0 0.3 DTPMP 0.4 0.4 0.2 0.4 Spray on Brightener  0.02 — —  0.02 C45E7 — — — 5.0 C45E2 2.5 2.5 2.0 — C45E3 2.6 2.5 2.0 — Perfume 0.5 0.3 0.5 0.2 Silicone antifoam 0.3 0.3 0.3 — Dry additives QEA — — — 1.0 EDDS 0.3 — — — Sulfate 2.0 3.0 5.0 10.0  Carbonate 6.0 13.0  15.0  14.0  Citric acid 2.5 — — 2.0 QAS II 0.5 — — 0.5 SKS-6 10.0  — — — Percarbonate 18.5  — — — PB4 — 18.0  10.0  21.5  NOBS 2.0 — — 2.0 DPDA — — — 1.0 DOBS — — 3.0 — NAC-OBS — 2.0 — — Protease 1.0 1.0 1.0 1.0 Lipase — 0.4 — 0.2 Lipase (1) 0.4 — 0.4 — Amylase 0.2 0.2 0.2 0.4 Brightener 1  0.05 — —  0.05 Misc/minor to 100%

EXAMPLE 3

The following granular detergent formulations are in accord with the invention.

K L M N O P Blown powder LAS 23.0  8.0 7.0 9.0 7.0 7.0 TAS — — — — 1.0 — C45AS 6.0 6.0 5.0 8.0 — — C45AE11S — 1.0 1.0 1.0 — — MES 2.0 — — — 2.0 4.0 Zeolite A 10.0  18.0  14.0  12.0  10.0  10.0  MA/AA — 0.5 — — — 2.0 MA/AA (1) 7.0 — — — — — AA — 3.0 3.0 2.0 3.0 3.0 Sulfate 5.0 6.3 14.3  11.0  15.0  19.3  Silicate 10.0  1.0 1.0 1.0 1.0 1.0 Carbonate 15.0  20.0  10.0  20.7  8.0 6.0 PEG 4000 0.4 1.5 1.5 1.0 1.0 1.0 DTPA — 0.9 0.5 — — 0.5 Brightener 2 0.3 0.2 0.3 — 0.1 0.3 Spray on C45E7 — 2.0 — — 2.0 2.0 C25E9 3.0 — — — — — C23E9 — — 1.5 2.0 — 2.0 Perfume 0.3 0.3 0.3 2.0 0.3 0.3 Agglomerates C45AS — 5.0 5.0 2.0 — 5.0 LAS — 2.0 2.0 — — 2.0 Zeolite A — 7.5 7.5 8.0 — 7.5 Carbonate — 4.0 4.0 5.0 — 4.0 PEG 4000 — 0.5 0.5 — — 0.5 Misc (water etc) — 2.0 2.0 2.0 — 2.0 Dry additives QAS (I) — — — — 1.0 — Citric acid — — — — 2.0 — PB4 — 3.0 — — 12.0  — PB1 4.0 1.0 3.0 2.0 — — Percarbonate — — — 2.0 — 10.0  Carbonate — 5.3 1.8 — 4.0 4.0 NOBS 4.0 — 1.0 2.0 — 0.6 DOBS — 3.0 — — 1.0 1.0 Methyl cellulose 0.2 — — — — — SKS-6 8.0 — — — — — STS — — 2.0 — 1.0 — Cumene sulfonic — 1.0 — — — 2.0 acid Lipase 0.2 — 0.2 — 0.2 0.4 Cellulase 0.2 0.2 0.2 0.3 0.2 0.2 Amylase 0.2 — 0.1 — 0.2 — Protease 0.5 0.5 0.5 0.3 0.5 0.5 PVPVI — — — — 0.5 0.1 PVP — — — — 0.5 — PVNO — — 0.5 0.3 — — QEA — — — — 1.0 — SRP1 0.2 0.5 0.3 — 0.2 — Silicone antifoam 0.2 0.4 0.2 0.4 0.1 — Mg sulfate — — 0.2 — 0.2 — Misc/minors to 100%

EXAMPLE 4

The following granular detergent formulations are in accord with the invention.

Q R S T Base granule STPP — 22.0  — 15.0  Zeolite A 30.0  — 24.0  5.0 Sulfate 10.0  5.0 10.0  7.0 MA/AA 3.0 — — — AA — 1.6 2.0 — MA/AA (1) — 12.0  — 6.0 LAS 14.0  10.0  9.0 20.0  C45AS 8.0 7.0 9.0 7.0 C45AE11S — 1.0 — 1.0 MES 0.5 4.0 6.0 — SADS 2.5 — — 1.0 Silicate — 1.0 0.5 10.0  Soap — 2.0 — — Brightener 1 0.2 0.2 0.2 0.2 Carbonate 6.0 9.0 10.0  10.0  PEG 4000 — 1.0 1.5 — DTPA — 0.4 — — Spray on C25E9 — — — 5.0 C45E7 1.0 1.0 — — C23E9 — 1.0 2.5 — Perfume 0.2 0.3 0.3 — Dry additives Carbonate 5.0 10.0  18.0  8.0 PVPVI/PVNO 0.5 — 0.3 — Protease 1.0 1.0 1.0 0.5 Lipase 0.4 — — 0.4 Amylase 0.1 — — 0.1 Cellulase 0.1 0.2 0.2 0.1 NOBS — 4.0 — 2.5 PB1 1.0 5.0 — 6.0 DOBS 3.0 — 1.0 — Percarbonate — — 5.0 — Sulfate 4.0 5.0 — 5.0 SRPI — 0.4 — — Sud supressor — 0.5 0.5 — Misc/minor to 100%

EXAMPLE 5

The following granular detergent compositions are in accord with the invention.

U V W Blown powder Zeolite A 20.0  — 15.0  STPP — 20.0  — Sulphate — — 5.0 Carbonate — — 5.0 TAS — — 1.0 LAS 6.0 6.0 6.0 MES 1.0 0.5 — SADE2S — 0.5 1.0 C68AS 2.0 2.0 — Silicate 3.0 8.0 — MA/AA 4.0 2.0 2.0 CMC 0.6 0.6 0.2 Brightener 1 0.2 0.2 0.1 DTPMP 0.4 0.4 0.1 STS — — 1.0 Spray on C45E7 5.0 5.0 4.0 Silicone antifoam 0.3 0.3 0.1 Perfume 0.2 0.2 0.3 Dry additives QEA — — 1.0 Carbonate 14.0  9.0 10.0  PB1 1.5 2.0 — PB4 18.5  13.0  13.0  NOBS 2.0 2.0 — DOBS — — 1.0 QAS (I) — — 1.0 Photoactivated bleach 15 ppm 15 ppm 15 ppm SKS-6 — — 3.0 Protease 1.0 1.0 0.2 Lipase 0.2 0.2 0.2 Amylase 0.4 0.4 0.2 Cellulase 0.1 0.1 0.2 Sulfate 10.0  20.0  5.0 Misc/minors to 100% Density (g/litre) 700    700    700   

EXAMPLE 6

The following detergent formulations are according to the present invention:

X Y Z AA BB CC LAS 18.0  14.0  24.0  20.0  18.0  16.0  QAS 0.7 1.0 — 0.7 0.5 0.5 TFAA — 1.0 — — — 1.0 C23E56.5 — — 1.0 — 1.0 1.0 C45E7 — 1.0 — — — — SADS — — — 1.0 3.0 0.5 SADE2S — — 5.0 1.0 — — MES 2.0 4.0 — — — 3.0 C45E3S 1.0 2.5 1.0 — 1.0 — STPP 32.0  18.0  30.0  22.0  15.0  24.0  Silicate 9.0 5.0 9.0 8.0 8.0 8.0 Carbonate 11.0  7.5 10.0  5.0 6.0 2.0 Bicarbonate — 7.5 — — — — PB1 3.0 1.0 1.0 — 7.0 — PB4 — 1.0 — — — 4.0 NOBS 2.0 1.0 0.5 — 1.0 — DTPMP — 1.0 — — 1.0 — DTPA 0.5 — 0.2 0.3 — 1.0 SRP 1 0.3 0.2 — 0.1 0.2 — MA/AA 1.0 1.5 2.0 0.5 0.8 0.8 CMC 0.8 0.4 0.4 0.2 0.5 0.5 PEI — — 0.4 — — 0.5 Sodium 20.0  10.0  20.0  30.0  15.0  15.0  sulfate Mg sulfate 0.2 — 0.4 0.9 0.5 0.5 Protease 0.8 1.0 0.5 0.5 0.5 0.8 Amylase 0.5 0.4 —  0.25 0.5 — Lipase 0.2 — 0.1 — — 0.3 Cellulase  0.15 — —  0.05 0.1 — Photoactivated 30 ppm 20 ppm — 10 ppm 10 ppm 10 ppm bleach (ppm) DOBS — — — — 2.0 1.0 DPDA — — — 1.0 — 1.0 Perfume 0.3 0.3 0.1 0.2 Brightener ½  0.05 0.2  0.08 0.1 Misc/minors to 100%

EXAMPLE 7

The following compositions are pre-treatment compositions in accordance with the invention.

DD EE FF GG HH II JJ MES 1.0 2.0 0.8 4.0 — — — C45E7 6.5 7.5 — — — — — C23E3 — 2.0 5.0 5.0 7.0 9.0 3.0 C25E2.5S 10.0 14.0 17.0 8.0 5.0 15.0 20.0 SADS — — 3.0 — 1.0 1.0 2.0 Acetyltriethyl 3.5 4.0 2.5 — — 3.0 3.5 citrate H2O2 4.0 2.0 6.0 7.0 2.0 3.0 0.8 NOBS 2.0 1.0 3.0 2.0 1.0 1.0 2.0 Water and minors H₂SO₄ up to pH 4 

What is claimed is:
 1. A detergent composition comprising (a) from 1% to 70%, by weight of a hydrophilic anionic surfactant system, comprising: (i) at least 50% by weight of the system one or more alkyl mono-sulphate and/or mono-sulphonate surfactants; and (I) a dianionic surfactants of the formula

 where R is an, optionally substituted, allyl, alkyl, alkenyl, aryl, akaryl, ether, ester, amine or amide group of chain length C₁ to C₂₈, or hydrogen; A and B are independently selected from alkylene, alkenylene, (poly)alkoxylene, hydroxyalkylene, arylalkylene or amido alkylene groups of chain length C₁ to C₂₈; whereby A, B, and R in total contain from 4 to about 31 carbon atoms; X and Y are anionic groups from the group comprising, carboxylate, sulfate and sulfonate, wherein at least one of X or Y is a sulfate group; z is 0 or 1; and M is a cationic counterion, said anionic surfactant system further optionally containing a member selected from the group consisting of; (ii) one or more additional anionic surfactants selected from the group consisting of: (II) an alkyl ester sulphonate surfactant of the formula R¹—CH(SO₃M)—(A)_(x)—C(O)—OR²  wherein R¹ is a C₆-C₂₂ hydrocarbyl, R² is a C₁-C₆ alkyl, A is a C₆-C₂₂ alkylene, alkenylene, x is 0 or 1, and M is a cation; and (III) an alkyl alkoxylated sulphate of the formula R⁵O(A)_(m)SO₄M  wherein R⁵ is a C₆-C₂₄ alkyl or hydroxyalkyl group, A is an alkoxy unit, the average of m is at least 5, and M is a cationic counterion; and b) from 0.01% to 10.0%, by weight of the composition of a hydrophobic bleaching system comprising (i) a peroxylic acid of the formula R¹—CO₃M  wherein R¹ has at least 6 carbon atoms, and M is a counterion; or (ii) a percarboxylic acid precursor of the formula R¹—CO—L  wherein L is a leaving group which is linked to the R¹—CO— group with an oxygen atom, and R¹ has at least 6 carbon atoms; or mixtures of (i) and (ii); wherein said percarboxylic acid or said percarboxylic acid precursor is derived from a parent carboxylic acid having a critical micelle concentration of less than 0.5 moles/liter wherein said critical micelle concentration is measured in aqueous solution at a temperature of 20° C.-50° C. and with the proviso that dianionic surfactant of formula (I) wherein R has 18 or 20 C-atoms, is present at a level of 2% or 2.7% by weight of the composition, the weight ratio of said dianionic surfactant to the hydrophobic bleaching agent is not 1:1 or 1.35:1.
 2. A detergent composition a to claim 1, wherein the bleaching system comprises a percarboxylic acid precursor, wherein L is an oxy benzene sulphonate and R¹ comprises 8 or 9 carbon atoms.
 3. A detergent composition according to claim 1 wherein the weight ratio of (a) to (b) is from 1:10 to 100:1.
 4. A detergent composition according to claim 1 wherein the bleaching system comprises a perborate or percarbonate salt, present at a level of from 2% to 30% by weight of the composition.
 5. A detergent composition according to claim 1 wherein the optional surfactant comprises an alkyl ester sulphonated surfactant of formula (II), having a R¹ C10-C22 alkyl, group.
 6. A detergent composition according to claim 1 wherein the dianionic surfactant (I) is selected from the group consisting of a 1,3 disulphate surfactant having from 7 to 23 C-atoms, and/or a 1,4 disulphate surfactant having from 8 to 22 C-atoms.
 7. A detergent composition according to claim 1 wherein the optional surfactant comprises an alkyl alkoxylated sulphate surfactant (III) having a value of m from 11 to
 20. 8. A detergent composition according to claim 1 wherein a quaternary ammonium surfactant or a nonionic surfactant is present.
 9. A detergent composition according to claim 1 comprising a phosphate-containing builder.
 10. A detergent composition according to claim 1 in the form of a solid detergent composition, having a bulk density of from 330 gr/liter to 600 gr/liter.
 11. A method of washing laundry by hand whereby a solid detergent composition according to claim 10 is used.
 12. A method of pre-treating or soaking of laundry with a detergent composition according to claim
 1. 13. A detergent composition according to claim 3 wherein the weight ratio of (a) to (b) is from 1:1 to 50:1. 